C0LGE4 · Y1124_ARATH
- ProteinProbable LRR receptor-like serine/threonine-protein kinase At1g12460
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids882 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score4/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_1_4247715_C_A | 5 | H>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: 1:g.4247715C>A Codon: CAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4247715C>A Locations: - p.His5Asn (EnsemblPlants:AT1G12460.1) - c.13C>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4247718_C_A | 6 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.37) Somatic: No Accession: 1:g.4247718C>A Codon: CTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4247718C>A Locations: - p.Leu6Ile (EnsemblPlants:AT1G12460.1) - c.16C>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11062041 | 13 | F>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.55) Somatic: No Accession: 1:g.4247741C>A Codon: TTC/TTA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4247741C>A Locations: - p.Phe13Leu (EnsemblPlants:AT1G12460.1) - c.39C>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11062042 | 22 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: 1:g.4247766G>A Codon: GAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4247766G>A Locations: - p.Asp22Asn (EnsemblPlants:AT1G12460.1) - c.64G>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04564983 | 23 | S>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 1:g.4247770C>T Codon: TCC/TTC Consequence type: missense Cytogenetic band: Genomic location: 1:g.4247770C>T Locations: - p.Ser23Phe (EnsemblPlants:AT1G12460.1) - c.68C>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00019885 | 38 | S>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.4247814A>T Codon: AGT/TGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4247814A>T Locations: - p.Ser38Cys (EnsemblPlants:AT1G12460.1) - c.112A>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04564984 | 43 | N>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.42) Somatic: No Accession: 1:g.4247830A>G Codon: AAC/AGC Consequence type: missense Cytogenetic band: Genomic location: 1:g.4247830A>G Locations: - p.Asn43Ser (EnsemblPlants:AT1G12460.1) - c.128A>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4247856_G_A | 52 | G>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.25) Somatic: No Accession: 1:g.4247856G>A Codon: GGT/AGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4247856G>A Locations: - p.Gly52Ser (EnsemblPlants:AT1G12460.1) - c.154G>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4247996_G_C | 98 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 1:g.4247996G>C Codon: TTG/TTC Consequence type: missense Cytogenetic band: Genomic location: 1:g.4247996G>C Locations: - p.Leu98Phe (EnsemblPlants:AT1G12460.1) - c.294G>C (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248019_A_T | 106 | N>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 1:g.4248019A>T Codon: AAT/ATT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248019A>T Locations: - p.Asn106Ile (EnsemblPlants:AT1G12460.1) - c.317A>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248024_C_G | 108 | P>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.4248024C>G Codon: CCG/GCG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248024C>G Locations: - p.Pro108Ala (EnsemblPlants:AT1G12460.1) - c.322C>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248087_G_T | 129 | G>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.4248087G>T Codon: GGT/TGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248087G>T Locations: - p.Gly129Cys (EnsemblPlants:AT1G12460.1) - c.385G>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248121_G_T | 140 | S>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 1:g.4248121G>T Codon: AGC/ATC Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248121G>T Locations: - p.Ser140Ile (EnsemblPlants:AT1G12460.1) - c.419G>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248128_G_T | 142 | R>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.4248128G>T Codon: AGG/AGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248128G>T Locations: - p.Arg142Ser (EnsemblPlants:AT1G12460.1) - c.426G>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11062043 | 143 | F>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.82) Somatic: No Accession: 1:g.4248129T>C Codon: TTT/CTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248129T>C Locations: - p.Phe143Leu (EnsemblPlants:AT1G12460.1) - c.427T>C (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248156_A_T | 152 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.4248156A>T Codon: ACC/TCC Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248156A>T Locations: - p.Thr152Ser (EnsemblPlants:AT1G12460.1) - c.454A>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04564988 | 179 | S>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 1:g.4248237T>G Codon: TCA/GCA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248237T>G Locations: - p.Ser179Ala (EnsemblPlants:AT1G12460.1) - c.535T>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248269_C_A | 189 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.96) Somatic: No Accession: 1:g.4248269C>A Codon: AAC/AAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248269C>A Locations: - p.Asn189Lys (EnsemblPlants:AT1G12460.1) - c.567C>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00019886 | 206 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.31) Somatic: No Accession: 1:g.4248319C>T Codon: CCT/CTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248319C>T Locations: - p.Pro206Leu (EnsemblPlants:AT1G12460.1) - c.617C>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11062044 | 208 | I>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 1:g.4248324A>T Codon: ATT/TTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248324A>T Locations: - p.Ile208Phe (EnsemblPlants:AT1G12460.1) - c.622A>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248361_G_A | 220 | R>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 1:g.4248361G>A Codon: AGA/AAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248361G>A Locations: - p.Arg220Lys (EnsemblPlants:AT1G12460.1) - c.659G>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248447_C_G | 249 | H>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.11) Somatic: No Accession: 1:g.4248447C>G Codon: CAT/GAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248447C>G Locations: - p.His249Asp (EnsemblPlants:AT1G12460.1) - c.745C>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248466_C_T | 255 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.22) Somatic: No Accession: 1:g.4248466C>T Codon: GCG/GTG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248466C>T Locations: - p.Ala255Val (EnsemblPlants:AT1G12460.1) - c.764C>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248487_T_C | 262 | I>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 1:g.4248487T>C Codon: ATA/ACA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248487T>C Locations: - p.Ile262Thr (EnsemblPlants:AT1G12460.1) - c.785T>C (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4248592_C_G | 297 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.95) Somatic: No Accession: 1:g.4248592C>G Codon: ACC/AGC Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248592C>G Locations: - p.Thr297Ser (EnsemblPlants:AT1G12460.1) - c.890C>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00019887 | 329 | G>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.11) Somatic: No Accession: 1:g.4248688G>T Codon: GGG/GTG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248688G>T Locations: - p.Gly329Val (EnsemblPlants:AT1G12460.1) - c.986G>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11062115 | 357 | F>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.4248772T>A Codon: TTT/TAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4248772T>A Locations: - p.Phe357Tyr (EnsemblPlants:AT1G12460.1) - c.1070T>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04564993 | 413 | R>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.77) Somatic: No Accession: 1:g.4249033G>A Codon: CGA/CAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249033G>A Locations: - p.Arg413Gln (EnsemblPlants:AT1G12460.1) - c.1238G>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4249111_C_T | 439 | S>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.47) Somatic: No Accession: 1:g.4249111C>T Codon: TCG/TTG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249111C>T Locations: - p.Ser439Leu (EnsemblPlants:AT1G12460.1) - c.1316C>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4249123_C_T | 443 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.26) Somatic: No Accession: 1:g.4249123C>T Codon: CCA/CTA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249123C>T Locations: - p.Pro443Leu (EnsemblPlants:AT1G12460.1) - c.1328C>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04564994 | 449 | G>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.4249140G>A Codon: GGG/AGG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249140G>A Locations: - p.Gly449Arg (EnsemblPlants:AT1G12460.1) - c.1345G>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04564994 | 449 | G>W | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.4249140G>T Codon: GGG/TGG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249140G>T Locations: - p.Gly449Trp (EnsemblPlants:AT1G12460.1) - c.1345G>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11062118 | 455 | T>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 1:g.4249159C>T Codon: ACG/ATG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249159C>T Locations: - p.Thr455Met (EnsemblPlants:AT1G12460.1) - c.1364C>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11062118 | 455 | T>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.17) Somatic: No Accession: 1:g.4249159C>G Codon: ACG/AGG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249159C>G Locations: - p.Thr455Arg (EnsemblPlants:AT1G12460.1) - c.1364C>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4249161_C_T | 456 | H>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.76) Somatic: No Accession: 1:g.4249161C>T Codon: CAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249161C>T Locations: - p.His456Tyr (EnsemblPlants:AT1G12460.1) - c.1366C>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01041610 | 491 | D>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 1:g.4249266G>T Codon: GAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249266G>T Locations: - p.Asp491Tyr (EnsemblPlants:AT1G12460.1) - c.1471G>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4249287_A_G | 498 | N>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.29) Somatic: No Accession: 1:g.4249287A>G Codon: AAT/GAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249287A>G Locations: - p.Asn498Asp (EnsemblPlants:AT1G12460.1) - c.1492A>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01041611 | 510 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.49) Somatic: No Accession: 1:g.4249323G>A Codon: GAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249323G>A Locations: - p.Asp510Asn (EnsemblPlants:AT1G12460.1) - c.1528G>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11062119 | 520 | I>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.4249353A>G Codon: ATT/GTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249353A>G Locations: - p.Ile520Val (EnsemblPlants:AT1G12460.1) - c.1558A>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04564996 | 543 | R>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.4249423G>T Codon: AGG/ATG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249423G>T Locations: - p.Arg543Met (EnsemblPlants:AT1G12460.1) - c.1628G>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4249495_T_G | 567 | I>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 1:g.4249495T>G Codon: ATA/AGA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249495T>G Locations: - p.Ile567Arg (EnsemblPlants:AT1G12460.1) - c.1700T>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13885855 | 610 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.4249623G>A Codon: GCA/ACA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249623G>A Locations: - p.Ala610Thr (EnsemblPlants:AT1G12460.1) - c.1828G>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00019888 | 616 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.69) Somatic: No Accession: 1:g.4249641G>A Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249641G>A Locations: - p.Val616Ile (EnsemblPlants:AT1G12460.1) - c.1846G>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11062122 | 683 | I>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.5) Somatic: No Accession: 1:g.4249842A>T Codon: ATT/TTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.4249842A>T Locations: - p.Ile683Phe (EnsemblPlants:AT1G12460.1) - c.2047A>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00019889 | 748 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.4250037T>A Codon: TTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4250037T>A Locations: - p.Leu748Ile (EnsemblPlants:AT1G12460.1) - c.2242T>A (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11062124 | 756 | D>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: 1:g.4250062A>G Codon: GAC/GGC Consequence type: missense Cytogenetic band: Genomic location: 1:g.4250062A>G Locations: - p.Asp756Gly (EnsemblPlants:AT1G12460.1) - c.2267A>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04565002 | 777 | Q>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.4250126G>C Codon: CAG/CAC Consequence type: missense Cytogenetic band: Genomic location: 1:g.4250126G>C Locations: - p.Gln777His (EnsemblPlants:AT1G12460.1) - c.2331G>C (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4250140_C_T | 782 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.53) Somatic: No Accession: 1:g.4250140C>T Codon: GCG/GTG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4250140C>T Locations: - p.Ala782Val (EnsemblPlants:AT1G12460.1) - c.2345C>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04565003 | 817 | R>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.27) Somatic: No Accession: 1:g.4250245G>C Codon: AGA/ACA Consequence type: missense Cytogenetic band: Genomic location: 1:g.4250245G>C Locations: - p.Arg817Thr (EnsemblPlants:AT1G12460.1) - c.2450G>C (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
tmp_1_4250248_A_G | 818 | D>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.4250248A>G Codon: GAC/GGC Consequence type: missense Cytogenetic band: Genomic location: 1:g.4250248A>G Locations: - p.Asp818Gly (EnsemblPlants:AT1G12460.1) - c.2453A>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04565005 | 856 | T>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.4250362C>T Codon: ACG/ATG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4250362C>T Locations: - p.Thr856Met (EnsemblPlants:AT1G12460.1) - c.2567C>T (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01041613 | 861 | L>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 1:g.4250377T>G Codon: CTG/CGG Consequence type: missense Cytogenetic band: Genomic location: 1:g.4250377T>G Locations: - p.Leu861Arg (EnsemblPlants:AT1G12460.1) - c.2582T>G (EnsemblPlants:AT1G12460.1) Source type: large scale study Cross-references: |