Q9XEC6 · CRK36_ARATH
- ProteinCysteine-rich receptor-like protein kinase 36
- GeneCRK36
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids658 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
ENSVATH09522672 | 3 | R>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.66) Somatic: No Accession: 4:g.2234631C>T Codon: AGA/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234631C>T Locations: - p.Arg3Lys (EnsemblPlants:AT4G04490.1) - c.8G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH09522670 | 5 | N>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.25) Somatic: No Accession: 4:g.2234625T>A Codon: AAT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234625T>A Locations: - p.Asn5Ile (EnsemblPlants:AT4G04490.1) - c.14A>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH09522671 | 5 | N>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.63) Somatic: No Accession: 4:g.2234626T>A Codon: AAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234626T>A Locations: - p.Asn5Tyr (EnsemblPlants:AT4G04490.1) - c.13A>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466915 | 8 | H>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.21) Somatic: No Accession: 4:g.2234616T>G Codon: CAC/CCC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234616T>G Locations: - p.His8Pro (EnsemblPlants:AT4G04490.1) - c.23A>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH08227128 | 10 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.87) Somatic: No Accession: 4:g.2234610G>A Codon: CCT/CTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234610G>A Locations: - p.Pro10Leu (EnsemblPlants:AT4G04490.1) - c.29C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13932262 | 15 | L>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 4:g.2234596A>C Codon: TTA/GTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234596A>C Locations: - p.Leu15Val (EnsemblPlants:AT4G04490.1) - c.43T>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234574_T_C | 22 | N>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.72) Somatic: No Accession: 4:g.2234574T>C Codon: AAT/AGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234574T>C Locations: - p.Asn22Ser (EnsemblPlants:AT4G04490.1) - c.65A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10717515 | 34 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.29) Somatic: No Accession: 4:g.2234537G>T Codon: GAC/GAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234537G>T Locations: - p.Asp34Glu (EnsemblPlants:AT4G04490.1) - c.102C>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466912 | 37 | P>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: 4:g.2234529G>C Codon: CCA/CGA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234529G>C Locations: - p.Pro37Arg (EnsemblPlants:AT4G04490.1) - c.110C>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652909 | 39 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.2234523G>A Codon: ACA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234523G>A Locations: - p.Thr39Ile (EnsemblPlants:AT4G04490.1) - c.116C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652909 | 39 | T>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.2234523G>T Codon: ACA/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234523G>T Locations: - p.Thr39Lys (EnsemblPlants:AT4G04490.1) - c.116C>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00462515 | 40 | S>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.2234520C>G Codon: AGC/ACC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234520C>G Locations: - p.Ser40Thr (EnsemblPlants:AT4G04490.1) - c.119G>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234515_C_T | 42 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.27) Somatic: No Accession: 4:g.2234515C>T Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234515C>T Locations: - p.Val42Ile (EnsemblPlants:AT4G04490.1) - c.124G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652907 | 53 | A>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2234481G>T Codon: GCT/GAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234481G>T Locations: - p.Ala53Asp (EnsemblPlants:AT4G04490.1) - c.158C>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234470_T_A | 57 | I>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 4:g.2234470T>A Codon: ATA/TTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234470T>A Locations: - p.Ile57Leu (EnsemblPlants:AT4G04490.1) - c.169A>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10717484 | 62 | F>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.2234453G>C Codon: TTC/TTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234453G>C Locations: - p.Phe62Leu (EnsemblPlants:AT4G04490.1) - c.186C>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00462514 | 64 | N>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2234449T>C Codon: AAC/GAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234449T>C Locations: - p.Asn64Asp (EnsemblPlants:AT4G04490.1) - c.190A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234428_A_G | 71 | Y>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 4:g.2234428A>G Codon: TAC/CAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234428A>G Locations: - p.Tyr71His (EnsemblPlants:AT4G04490.1) - c.211T>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652904 | 101 | R>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.28) Somatic: No Accession: 4:g.2234337C>T Codon: CGA/CAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234337C>T Locations: - p.Arg101Gln (EnsemblPlants:AT4G04490.1) - c.302G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10717482 | 104 | T>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 4:g.2234328G>T Codon: ACA/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234328G>T Locations: - p.Thr104Lys (EnsemblPlants:AT4G04490.1) - c.311C>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234322_G_A | 106 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.2234322G>A Codon: GCA/GTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234322G>A Locations: - p.Ala106Val (EnsemblPlants:AT4G04490.1) - c.317C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466909 | 111 | S>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.2234307G>A Codon: TCC/TTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234307G>A Locations: - p.Ser111Phe (EnsemblPlants:AT4G04490.1) - c.332C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234292_T_G | 116 | N>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 4:g.2234292T>G Codon: AAC/ACC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234292T>G Locations: - p.Asn116Thr (EnsemblPlants:AT4G04490.1) - c.347A>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234283_C_T | 119 | C>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2234283C>T Codon: TGT/TAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234283C>T Locations: - p.Cys119Tyr (EnsemblPlants:AT4G04490.1) - c.356G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234278_C_T | 121 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 4:g.2234278C>T Codon: GTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234278C>T Locations: - p.Val121Ile (EnsemblPlants:AT4G04490.1) - c.361G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10717480 | 128 | R>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.84) Somatic: No Accession: 4:g.2234255T>A Codon: AGA/AGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234255T>A Locations: - p.Arg128Ser (EnsemblPlants:AT4G04490.1) - c.384A>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652902 | 128 | R>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.77) Somatic: No Accession: 4:g.2234256C>G Codon: AGA/ACA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234256C>G Locations: - p.Arg128Thr (EnsemblPlants:AT4G04490.1) - c.383G>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234232_G_C | 136 | P>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2234232G>C Codon: CCA/CGA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234232G>C Locations: - p.Pro136Arg (EnsemblPlants:AT4G04490.1) - c.407C>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466908 | 136 | P>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 4:g.2234233G>A Codon: CCA/TCA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234233G>A Locations: - p.Pro136Ser (EnsemblPlants:AT4G04490.1) - c.406C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00462509 | 140 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 4:g.2234220A>G Codon: GTT/GCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234220A>G Locations: - p.Val140Ala (EnsemblPlants:AT4G04490.1) - c.419T>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466905 | 149 | S>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 4:g.2234193G>A Codon: TCC/TTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234193G>A Locations: - p.Ser149Phe (EnsemblPlants:AT4G04490.1) - c.446C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466904 | 152 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.2234184G>C Codon: ACC/AGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234184G>C Locations: - p.Thr152Ser (EnsemblPlants:AT4G04490.1) - c.455C>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00462507 | 163 | N>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.22) Somatic: No Accession: 4:g.2234151T>C Codon: AAT/AGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234151T>C Locations: - p.Asn163Ser (EnsemblPlants:AT4G04490.1) - c.488A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13932260 | 166 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.89) Somatic: No Accession: 4:g.2234143C>T Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234143C>T Locations: - p.Val166Ile (EnsemblPlants:AT4G04490.1) - c.496G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234112_G_A | 176 | S>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.2234112G>A Codon: TCG/TTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234112G>A Locations: - p.Ser176Leu (EnsemblPlants:AT4G04490.1) - c.527C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466902 ENSVATH06466903 | 185 | S>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.58) Somatic: No Accession: 4:g.2234084A>C, 4:g.2234086T>G Codon: AGT/AGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234084A>C, 4:g.2234086T>G Locations: - p.Ser185Arg (EnsemblPlants:AT4G04490.1) - c.555T>G (EnsemblPlants:AT4G04490.1) - c.553A>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466901 | 187 | E>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 4:g.2234080C>G Codon: GAG/CAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234080C>G Locations: - p.Glu187Gln (EnsemblPlants:AT4G04490.1) - c.559G>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234067_G_C | 191 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 4:g.2234067G>C Codon: ACT/AGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234067G>C Locations: - p.Thr191Ser (EnsemblPlants:AT4G04490.1) - c.572C>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234022_G_A | 206 | S>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2234022G>A Codon: TCC/TTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234022G>A Locations: - p.Ser206Phe (EnsemblPlants:AT4G04490.1) - c.617C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2234004_C_T | 212 | C>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2234004C>T Codon: TGT/TAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2234004C>T Locations: - p.Cys212Tyr (EnsemblPlants:AT4G04490.1) - c.635G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2233941_G_T | 233 | A>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.21) Somatic: No Accession: 4:g.2233941G>T Codon: GCC/GAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233941G>T Locations: - p.Ala233Asp (EnsemblPlants:AT4G04490.1) - c.698C>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10717476 | 233 | A>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 4:g.2233942C>A Codon: GCC/TCC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233942C>A Locations: - p.Ala233Ser (EnsemblPlants:AT4G04490.1) - c.697G>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652897 | 256 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.28) Somatic: No Accession: 4:g.2233872A>G Codon: GTT/GCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233872A>G Locations: - p.Val256Ala (EnsemblPlants:AT4G04490.1) - c.767T>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2233866_G_A | 258 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.05) Somatic: No Accession: 4:g.2233866G>A Codon: GCG/GTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233866G>A Locations: - p.Ala258Val (EnsemblPlants:AT4G04490.1) - c.773C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466899 | 260 | P>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: 4:g.2233861G>A Codon: CCT/TCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233861G>A Locations: - p.Pro260Ser (EnsemblPlants:AT4G04490.1) - c.778C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652896 | 261 | R>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.59) Somatic: No Accession: 4:g.2233857C>T Codon: CGA/CAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233857C>T Locations: - p.Arg261Gln (EnsemblPlants:AT4G04490.1) - c.782G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652895 | 262 | S>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.2233855A>G Codon: TCT/CCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233855A>G Locations: - p.Ser262Pro (EnsemblPlants:AT4G04490.1) - c.784T>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652893 | 265 | T>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.33) Somatic: No Accession: 4:g.2233846T>G Codon: ACT/CCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233846T>G Locations: - p.Thr265Pro (EnsemblPlants:AT4G04490.1) - c.793A>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00462503 | 269 | Y>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.2233833T>G Codon: TAT/TCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233833T>G Locations: - p.Tyr269Ser (EnsemblPlants:AT4G04490.1) - c.806A>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2233831_G_A | 270 | R>W | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 4:g.2233831G>A Codon: CGG/TGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233831G>A Locations: - p.Arg270Trp (EnsemblPlants:AT4G04490.1) - c.808C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10717404 | 271 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.21) Somatic: No Accession: 4:g.2233828C>T Codon: GTC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233828C>T Locations: - p.Val271Ile (EnsemblPlants:AT4G04490.1) - c.811G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652889 | 276 | M>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.34) Somatic: No Accession: 4:g.2233750C>A, 4:g.2233750C>T Codon: ATG/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233750C>A, 4:g.2233750C>T Locations: - p.Met276Ile (EnsemblPlants:AT4G04490.1) - c.828G>T (EnsemblPlants:AT4G04490.1) - c.828G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652890 | 276 | M>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: 4:g.2233752T>C Codon: ATG/GTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233752T>C Locations: - p.Met276Val (EnsemblPlants:AT4G04490.1) - c.826A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466897 | 277 | F>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.46) Somatic: No Accession: 4:g.2233749A>G Codon: TTT/CTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233749A>G Locations: - p.Phe277Leu (EnsemblPlants:AT4G04490.1) - c.829T>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2233737_T_C | 281 | S>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.5) Somatic: No Accession: 4:g.2233737T>C Codon: AGC/GGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233737T>C Locations: - p.Ser281Gly (EnsemblPlants:AT4G04490.1) - c.841A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652886 | 290 | G>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.2233709C>A Codon: GGC/GTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233709C>A Locations: - p.Gly290Val (EnsemblPlants:AT4G04490.1) - c.869G>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652885 | 291 | I>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: 4:g.2233707T>C Codon: ATA/GTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233707T>C Locations: - p.Ile291Val (EnsemblPlants:AT4G04490.1) - c.871A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652883 | 295 | V>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 4:g.2233695C>T Codon: GTG/ATG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233695C>T Locations: - p.Val295Met (EnsemblPlants:AT4G04490.1) - c.883G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00462502 | 304 | R>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.4) Somatic: No Accession: 4:g.2233668G>C Codon: CGC/GGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233668G>C Locations: - p.Arg304Gly (EnsemblPlants:AT4G04490.1) - c.910C>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652880 | 312 | T>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.93) Somatic: No Accession: 4:g.2233644T>C Codon: ACT/GCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233644T>C Locations: - p.Thr312Ala (EnsemblPlants:AT4G04490.1) - c.934A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652879 | 316 | K>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.2233632T>C Codon: AAG/GAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233632T>C Locations: - p.Lys316Glu (EnsemblPlants:AT4G04490.1) - c.946A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10717395 | 328 | F>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2233514A>C Codon: TTT/GTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233514A>C Locations: - p.Phe328Val (EnsemblPlants:AT4G04490.1) - c.982T>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466892 | 330 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.2233508G>T Codon: CTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233508G>T Locations: - p.Leu330Ile (EnsemblPlants:AT4G04490.1) - c.988C>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652870 | 339 | E>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.44) Somatic: No Accession: 4:g.2233481C>T Codon: GAG/AAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233481C>T Locations: - p.Glu339Lys (EnsemblPlants:AT4G04490.1) - c.1015G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652868 | 342 | L>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.33) Somatic: No Accession: 4:g.2233471A>G Codon: CTT/CCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233471A>G Locations: - p.Leu342Pro (EnsemblPlants:AT4G04490.1) - c.1025T>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2233337_C_A | 361 | S>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2233337C>A Codon: AGC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233337C>A Locations: - p.Ser361Ile (EnsemblPlants:AT4G04490.1) - c.1082G>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2233305_C_A | 372 | G>* | 1000Genomes | ||||
Consequence: stop gained Somatic: No Accession: 4:g.2233305C>A Codon: GGA/TGA Consequence type: stop gained Cytogenetic band: Genomic location: 4:g.2233305C>A Locations: - p.Gly372Ter (EnsemblPlants:AT4G04490.1) - c.1114G>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652857 | 372 | G>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.2233304C>T Codon: GGA/GAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233304C>T Locations: - p.Gly372Glu (EnsemblPlants:AT4G04490.1) - c.1115G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2233275_T_G | 382 | K>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2233275T>G Codon: AAG/CAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233275T>G Locations: - p.Lys382Gln (EnsemblPlants:AT4G04490.1) - c.1144A>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466890 | 400 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2233221G>T Codon: CTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233221G>T Locations: - p.Leu400Ile (EnsemblPlants:AT4G04490.1) - c.1198C>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652856 | 404 | N>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.7) Somatic: No Accession: 4:g.2233208T>G Codon: AAT/ACT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233208T>G Locations: - p.Asn404Thr (EnsemblPlants:AT4G04490.1) - c.1211A>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2233069_T_C | 427 | D>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.2233069T>C Codon: GAC/GGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233069T>C Locations: - p.Asp427Gly (EnsemblPlants:AT4G04490.1) - c.1280A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13932255 | 430 | K>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 4:g.2233059T>G Codon: AAA/AAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2233059T>G Locations: - p.Lys430Asn (EnsemblPlants:AT4G04490.1) - c.1290A>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232960_G_C | 463 | H>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2232960G>C Codon: CAC/CAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232960G>C Locations: - p.His463Gln (EnsemblPlants:AT4G04490.1) - c.1389C>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232935_G_A | 472 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2232935G>A Codon: CTT/TTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232935G>A Locations: - p.Leu472Phe (EnsemblPlants:AT4G04490.1) - c.1414C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232930_T_G | 473 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2232930T>G Codon: TTA/TTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232930T>G Locations: - p.Leu473Phe (EnsemblPlants:AT4G04490.1) - c.1419A>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10717352 | 475 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.2232925G>A Codon: GCG/GTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232925G>A Locations: - p.Ala475Val (EnsemblPlants:AT4G04490.1) - c.1424C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232915_G_T | 478 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2232915G>T Codon: AAC/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232915G>T Locations: - p.Asn478Lys (EnsemblPlants:AT4G04490.1) - c.1434C>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466886 | 481 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.74) Somatic: No Accession: 4:g.2232908C>T Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232908C>T Locations: - p.Val481Ile (EnsemblPlants:AT4G04490.1) - c.1441G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466885 | 491 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 4:g.2232876G>T Codon: AAC/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232876G>T Locations: - p.Asn491Lys (EnsemblPlants:AT4G04490.1) - c.1473C>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232854_T_C | 499 | T>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2232854T>C Codon: ACA/GCA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232854T>C Locations: - p.Thr499Ala (EnsemblPlants:AT4G04490.1) - c.1495A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232744_G_A | 511 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2232744G>A Codon: CCG/CTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232744G>A Locations: - p.Pro511Leu (EnsemblPlants:AT4G04490.1) - c.1532C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232714_G_A | 521 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.21) Somatic: No Accession: 4:g.2232714G>A Codon: GCT/GTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232714G>A Locations: - p.Ala521Val (EnsemblPlants:AT4G04490.1) - c.1562C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13932223 | 525 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 4:g.2232703C>T Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232703C>T Locations: - p.Val525Ile (EnsemblPlants:AT4G04490.1) - c.1573G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466882 | 532 | L>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.49) Somatic: No Accession: 4:g.2232682G>C Codon: CTT/GTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232682G>C Locations: - p.Leu532Val (EnsemblPlants:AT4G04490.1) - c.1594C>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10717232 | 554 | W>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2232273C>G Codon: TGG/TCG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232273C>G Locations: - p.Trp554Ser (EnsemblPlants:AT4G04490.1) - c.1661G>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652789 | 558 | I>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.51) Somatic: No Accession: 4:g.2232262T>C Codon: ATA/GTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232262T>C Locations: - p.Ile558Val (EnsemblPlants:AT4G04490.1) - c.1672A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232259_C_T | 559 | E>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.14) Somatic: No Accession: 4:g.2232259C>T Codon: GAA/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232259C>T Locations: - p.Glu559Lys (EnsemblPlants:AT4G04490.1) - c.1675G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232256_C_A | 560 | G>* | 1000Genomes | ||||
Consequence: stop gained Somatic: No Accession: 4:g.2232256C>A Codon: GGA/TGA Consequence type: stop gained Cytogenetic band: Genomic location: 4:g.2232256C>A Locations: - p.Gly560Ter (EnsemblPlants:AT4G04490.1) - c.1678G>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232253_C_T | 561 | E>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.2232253C>T Codon: GAG/AAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232253C>T Locations: - p.Glu561Lys (EnsemblPlants:AT4G04490.1) - c.1681G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466866 | 579 | I>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.58) Somatic: No Accession: 4:g.2232198A>G Codon: ATA/ACA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232198A>G Locations: - p.Ile579Thr (EnsemblPlants:AT4G04490.1) - c.1736T>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232168_A_G | 589 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 4:g.2232168A>G Codon: GTT/GCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232168A>G Locations: - p.Val589Ala (EnsemblPlants:AT4G04490.1) - c.1766T>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466864 | 592 | N>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2232160T>G Codon: AAT/CAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232160T>G Locations: - p.Asn592His (EnsemblPlants:AT4G04490.1) - c.1774A>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13932194 | 594 | A>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.14) Somatic: No Accession: 4:g.2232153G>T Codon: GCA/GAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232153G>T Locations: - p.Ala594Glu (EnsemblPlants:AT4G04490.1) - c.1781C>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13932193 | 598 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.2232141G>A Codon: ACC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232141G>A Locations: - p.Thr598Ile (EnsemblPlants:AT4G04490.1) - c.1793C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652787 | 599 | M>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 4:g.2232137C>T Codon: ATG/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232137C>T Locations: - p.Met599Ile (EnsemblPlants:AT4G04490.1) - c.1797G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652786 | 600 | N>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.2232136T>A Codon: AAC/TAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232136T>A Locations: - p.Asn600Tyr (EnsemblPlants:AT4G04490.1) - c.1798A>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232127_T_A | 603 | I>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 4:g.2232127T>A Codon: ATA/TTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232127T>A Locations: - p.Ile603Leu (EnsemblPlants:AT4G04490.1) - c.1807A>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232123_G_C | 604 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.2232123G>C Codon: ACT/AGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232123G>C Locations: - p.Thr604Ser (EnsemblPlants:AT4G04490.1) - c.1811C>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00462493 | 609 | D>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.18) Somatic: No Accession: 4:g.2232109C>G Codon: GAC/CAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232109C>G Locations: - p.Asp609His (EnsemblPlants:AT4G04490.1) - c.1825G>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2232088_T_C | 616 | K>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.05) Somatic: No Accession: 4:g.2232088T>C Codon: AAA/GAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232088T>C Locations: - p.Lys616Glu (EnsemblPlants:AT4G04490.1) - c.1846A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466862 | 618 | T>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: 4:g.2232082T>C Codon: ACA/GCA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232082T>C Locations: - p.Thr618Ala (EnsemblPlants:AT4G04490.1) - c.1852A>G (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466861 | 618 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.2232081G>A Codon: ACA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232081G>A Locations: - p.Thr618Ile (EnsemblPlants:AT4G04490.1) - c.1853C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06466860 | 623 | V>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.85) Somatic: No Accession: 4:g.2232067C>G Codon: GTC/CTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232067C>G Locations: - p.Val623Leu (EnsemblPlants:AT4G04490.1) - c.1867G>C (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652783 | 624 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.42) Somatic: No Accession: 4:g.2232063G>A Codon: ACT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232063G>A Locations: - p.Thr624Ile (EnsemblPlants:AT4G04490.1) - c.1871C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00462492 | 628 | S>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: 4:g.2232051G>A Codon: TCG/TTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232051G>A Locations: - p.Ser628Leu (EnsemblPlants:AT4G04490.1) - c.1883C>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02652782 | 629 | V>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.23) Somatic: No Accession: 4:g.2232049C>T Codon: GTG/ATG Consequence type: missense Cytogenetic band: Genomic location: 4:g.2232049C>T Locations: - p.Val629Met (EnsemblPlants:AT4G04490.1) - c.1885G>A (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: | |||||||
tmp_4_2231977_T_A | 653 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.2) Somatic: No Accession: 4:g.2231977T>A Codon: ACA/TCA Consequence type: missense Cytogenetic band: Genomic location: 4:g.2231977T>A Locations: - p.Thr653Ser (EnsemblPlants:AT4G04490.1) - c.1957A>T (EnsemblPlants:AT4G04490.1) Source type: large scale study Cross-references: |