O23349 · AO1_ARATH
- ProteinPrimary amine oxidase 1
- GeneAO1
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids650 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_4_8541886_C_A | 3 | T>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.14) Somatic: No Accession: 4:g.8541886C>A Codon: ACA/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8541886C>A Locations: - p.Thr3Lys (EnsemblPlants:AT4G14940.1) - c.8C>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8541918_T_G | 14 | C>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 4:g.8541918T>G Codon: TGT/GGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8541918T>G Locations: - p.Cys14Gly (EnsemblPlants:AT4G14940.1) - c.40T>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8541922_T_C | 15 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.6) Somatic: No Accession: 4:g.8541922T>C Codon: GTT/GCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8541922T>C Locations: - p.Val15Ala (EnsemblPlants:AT4G14940.1) - c.44T>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669122 | 20 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.73) Somatic: No Accession: 4:g.8541936C>T Codon: CTC/TTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8541936C>T Locations: - p.Leu20Phe (EnsemblPlants:AT4G14940.1) - c.58C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669122 | 20 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.41) Somatic: No Accession: 4:g.8541936C>A Codon: CTC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8541936C>A Locations: - p.Leu20Ile (EnsemblPlants:AT4G14940.1) - c.58C>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669123 | 31 | Q>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: 4:g.8541970A>G Codon: CAA/CGA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8541970A>G Locations: - p.Gln31Arg (EnsemblPlants:AT4G14940.1) - c.92A>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8541974_A_T | 32 | E>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8541974A>T Codon: GAA/GAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8541974A>T Locations: - p.Glu32Asp (EnsemblPlants:AT4G14940.1) - c.96A>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8541991_T_A | 38 | F>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 4:g.8541991T>A Codon: TTT/TAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8541991T>A Locations: - p.Phe38Tyr (EnsemblPlants:AT4G14940.1) - c.113T>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8541993_A_C | 39 | I>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.16) Somatic: No Accession: 4:g.8541993A>C Codon: ATC/CTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8541993A>C Locations: - p.Ile39Leu (EnsemblPlants:AT4G14940.1) - c.115A>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669124 | 40 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.66) Somatic: No Accession: 4:g.8541996G>A Codon: GTC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8541996G>A Locations: - p.Val40Ile (EnsemblPlants:AT4G14940.1) - c.118G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542000_A_G | 41 | K>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.55) Somatic: No Accession: 4:g.8542000A>G Codon: AAG/AGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542000A>G Locations: - p.Lys41Arg (EnsemblPlants:AT4G14940.1) - c.122A>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11752937 | 44 | H>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8542008C>T Codon: CAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542008C>T Locations: - p.His44Tyr (EnsemblPlants:AT4G14940.1) - c.130C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542020_C_T | 48 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.67) Somatic: No Accession: 4:g.8542020C>T Codon: CTC/TTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542020C>T Locations: - p.Leu48Phe (EnsemblPlants:AT4G14940.1) - c.142C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542026_G_A | 50 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8542026G>A Codon: GAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542026G>A Locations: - p.Asp50Asn (EnsemblPlants:AT4G14940.1) - c.148G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14196624 | 64 | S>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 4:g.8542070C>G Codon: AGC/AGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542070C>G Locations: - p.Ser64Arg (EnsemblPlants:AT4G14940.1) - c.192C>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542073_C_A | 65 | H>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.59) Somatic: No Accession: 4:g.8542073C>A Codon: CAC/CAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542073C>A Locations: - p.His65Gln (EnsemblPlants:AT4G14940.1) - c.195C>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14196645 | 66 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: 4:g.8542074G>A Codon: GTC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542074G>A Locations: - p.Val66Ile (EnsemblPlants:AT4G14940.1) - c.196G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669126 | 68 | Q>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 4:g.8542081A>T Codon: CAA/CTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542081A>T Locations: - p.Gln68Leu (EnsemblPlants:AT4G14940.1) - c.203A>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542110_C_T | 78 | P>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.56) Somatic: No Accession: 4:g.8542110C>T Codon: CCA/TCA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542110C>T Locations: - p.Pro78Ser (EnsemblPlants:AT4G14940.1) - c.232C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836083 | 80 | P>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.45) Somatic: No Accession: 4:g.8542117C>G Codon: CCC/CGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542117C>G Locations: - p.Pro80Arg (EnsemblPlants:AT4G14940.1) - c.239C>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836084 | 91 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.4) Somatic: No Accession: 4:g.8542149G>A Codon: GCC/ACC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542149G>A Locations: - p.Ala91Thr (EnsemblPlants:AT4G14940.1) - c.271G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542164_T_C | 96 | Y>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8542164T>C Codon: TAC/CAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542164T>C Locations: - p.Tyr96His (EnsemblPlants:AT4G14940.1) - c.286T>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542170_C_A | 98 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 4:g.8542170C>A Codon: CTC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542170C>A Locations: - p.Leu98Ile (EnsemblPlants:AT4G14940.1) - c.292C>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542174_T_C | 99 | I>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.99) Somatic: No Accession: 4:g.8542174T>C Codon: ATC/ACC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542174T>C Locations: - p.Ile99Thr (EnsemblPlants:AT4G14940.1) - c.296T>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836085 | 103 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.8542186C>T Codon: ACC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542186C>T Locations: - p.Thr103Ile (EnsemblPlants:AT4G14940.1) - c.308C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542196_G_C | 106 | K>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 4:g.8542196G>C Codon: AAG/AAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542196G>C Locations: - p.Lys106Asn (EnsemblPlants:AT4G14940.1) - c.318G>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542215_T_A | 113 | Y>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: 4:g.8542215T>A Codon: TAC/AAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542215T>A Locations: - p.Tyr113Asn (EnsemblPlants:AT4G14940.1) - c.337T>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14196646 | 114 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 4:g.8542219C>T Codon: ACA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542219C>T Locations: - p.Thr114Ile (EnsemblPlants:AT4G14940.1) - c.341C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542248_A_T | 124 | I>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 4:g.8542248A>T Codon: ATA/TTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542248A>T Locations: - p.Ile124Leu (EnsemblPlants:AT4G14940.1) - c.370A>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542273_T_A | 132 | L>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542273T>A Codon: CTT/CAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542273T>A Locations: - p.Leu132His (EnsemblPlants:AT4G14940.1) - c.395T>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542359_G_C | 161 | G>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542359G>C Codon: GGT/CGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542359G>C Locations: - p.Gly161Arg (EnsemblPlants:AT4G14940.1) - c.481G>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669131 | 167 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.26) Somatic: No Accession: 4:g.8542377A>T Codon: ACC/TCC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542377A>T Locations: - p.Thr167Ser (EnsemblPlants:AT4G14940.1) - c.499A>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669132 | 168 | T>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: 4:g.8542381C>G Codon: ACG/AGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542381C>G Locations: - p.Thr168Arg (EnsemblPlants:AT4G14940.1) - c.503C>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542409_T_A | 177 | F>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.8542409T>A Codon: TTT/TTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542409T>A Locations: - p.Phe177Leu (EnsemblPlants:AT4G14940.1) - c.531T>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836093 | 188 | R>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542441G>T Codon: AGA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542441G>T Locations: - p.Arg188Ile (EnsemblPlants:AT4G14940.1) - c.563G>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00505716 | 195 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.94) Somatic: No Accession: 4:g.8542461G>A Codon: GTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542461G>A Locations: - p.Val195Ile (EnsemblPlants:AT4G14940.1) - c.583G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836097 | 205 | I>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542493C>G Codon: ATC/ATG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542493C>G Locations: - p.Ile205Met (EnsemblPlants:AT4G14940.1) - c.615C>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836096 | 205 | I>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8542491A>G Codon: ATC/GTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542491A>G Locations: - p.Ile205Val (EnsemblPlants:AT4G14940.1) - c.613A>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836098 | 215 | I>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.35) Somatic: No Accession: 4:g.8542521A>C Codon: ATC/CTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542521A>C Locations: - p.Ile215Leu (EnsemblPlants:AT4G14940.1) - c.643A>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836099 | 217 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 4:g.8542529T>G, 4:g.8542529T>A Codon: GAT/GAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542529T>G, 4:g.8542529T>A Locations: - p.Asp217Glu (EnsemblPlants:AT4G14940.1) - c.651T>G (EnsemblPlants:AT4G14940.1) - c.651T>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669135 | 217 | D>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542527G>C Codon: GAT/CAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542527G>C Locations: - p.Asp217His (EnsemblPlants:AT4G14940.1) - c.649G>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669136 | 218 | K>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542530A>G Codon: AAA/GAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542530A>G Locations: - p.Lys218Glu (EnsemblPlants:AT4G14940.1) - c.652A>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542557_C_T | 227 | H>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.8542557C>T Codon: CAC/TAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542557C>T Locations: - p.His227Tyr (EnsemblPlants:AT4G14940.1) - c.679C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836102 | 228 | R>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.65) Somatic: No Accession: 4:g.8542561G>A Codon: AGA/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542561G>A Locations: - p.Arg228Lys (EnsemblPlants:AT4G14940.1) - c.683G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836103 | 229 | P>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.54) Somatic: No Accession: 4:g.8542563C>G Codon: CCC/GCC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542563C>G Locations: - p.Pro229Ala (EnsemblPlants:AT4G14940.1) - c.685C>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836103 | 229 | P>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.42) Somatic: No Accession: 4:g.8542563C>A Codon: CCC/ACC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542563C>A Locations: - p.Pro229Thr (EnsemblPlants:AT4G14940.1) - c.685C>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00505718 | 233 | F>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.58) Somatic: No Accession: 4:g.8542576T>C Codon: TTT/TCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542576T>C Locations: - p.Phe233Ser (EnsemblPlants:AT4G14940.1) - c.698T>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669137 | 235 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.65) Somatic: No Accession: 4:g.8542583C>A Codon: AAC/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542583C>A Locations: - p.Asn235Lys (EnsemblPlants:AT4G14940.1) - c.705C>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669139 | 245 | G>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542611G>A Codon: GGC/AGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542611G>A Locations: - p.Gly245Ser (EnsemblPlants:AT4G14940.1) - c.733G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669141 | 252 | N>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.8542633A>C Codon: AAC/ACC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542633A>C Locations: - p.Asn252Thr (EnsemblPlants:AT4G14940.1) - c.755A>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669142 | 260 | T>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542656A>G Codon: ACC/GCC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542656A>G Locations: - p.Thr260Ala (EnsemblPlants:AT4G14940.1) - c.778A>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669143 | 266 | T>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542674A>G Codon: ACT/GCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542674A>G Locations: - p.Thr266Ala (EnsemblPlants:AT4G14940.1) - c.796A>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836105 | 279 | R>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8542714G>A Codon: AGG/AAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542714G>A Locations: - p.Arg279Lys (EnsemblPlants:AT4G14940.1) - c.836G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836105 | 279 | R>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.8542714G>T Codon: AGG/ATG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542714G>T Locations: - p.Arg279Met (EnsemblPlants:AT4G14940.1) - c.836G>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542777_C_G | 300 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.35) Somatic: No Accession: 4:g.8542777C>G Codon: ACC/AGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542777C>G Locations: - p.Thr300Ser (EnsemblPlants:AT4G14940.1) - c.899C>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669144 | 304 | Y>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542788T>C Codon: TAC/CAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542788T>C Locations: - p.Tyr304His (EnsemblPlants:AT4G14940.1) - c.910T>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542849_A_G | 324 | Q>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.45) Somatic: No Accession: 4:g.8542849A>G Codon: CAG/CGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542849A>G Locations: - p.Gln324Arg (EnsemblPlants:AT4G14940.1) - c.971A>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00505725 | 336 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: 4:g.8542886A>T Codon: TTA/TTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542886A>T Locations: - p.Leu336Phe (EnsemblPlants:AT4G14940.1) - c.1008A>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669146 | 337 | D>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542887G>T Codon: GAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542887G>T Locations: - p.Asp337Tyr (EnsemblPlants:AT4G14940.1) - c.1009G>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836106 | 338 | G>W | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8542890G>T Codon: GGG/TGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542890G>T Locations: - p.Gly338Trp (EnsemblPlants:AT4G14940.1) - c.1012G>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669147 | 339 | H>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 4:g.8542894A>T Codon: CAC/CTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542894A>T Locations: - p.His339Leu (EnsemblPlants:AT4G14940.1) - c.1016A>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542902_G_A | 342 | G>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.8542902G>A Codon: GGA/AGA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542902G>A Locations: - p.Gly342Arg (EnsemblPlants:AT4G14940.1) - c.1024G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8542939_T_C | 354 | M>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 4:g.8542939T>C Codon: ATG/ACG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542939T>C Locations: - p.Met354Thr (EnsemblPlants:AT4G14940.1) - c.1061T>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669148 | 356 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8542944G>A Codon: GTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542944G>A Locations: - p.Val356Ile (EnsemblPlants:AT4G14940.1) - c.1066G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14196648 | 360 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.8542958C>A Codon: AAC/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542958C>A Locations: - p.Asn360Lys (EnsemblPlants:AT4G14940.1) - c.1080C>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11752942 | 369 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.8542984C>T Codon: ACC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8542984C>T Locations: - p.Thr369Ile (EnsemblPlants:AT4G14940.1) - c.1106C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8543142_C_T | 394 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.8543142C>T Codon: ACA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543142C>T Locations: - p.Thr394Ile (EnsemblPlants:AT4G14940.1) - c.1181C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11753021 | 402 | V>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8543166T>G Codon: GTG/GGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543166T>G Locations: - p.Val402Gly (EnsemblPlants:AT4G14940.1) - c.1205T>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11753022 | 406 | F>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8543177T>A Codon: TTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543177T>A Locations: - p.Phe406Ile (EnsemblPlants:AT4G14940.1) - c.1216T>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00505729 | 426 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8543512C>T Codon: GCG/GTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543512C>T Locations: - p.Ala426Val (EnsemblPlants:AT4G14940.1) - c.1277C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02836125 | 433 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.11) Somatic: No Accession: 4:g.8543534T>G Codon: GAT/GAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543534T>G Locations: - p.Asp433Glu (EnsemblPlants:AT4G14940.1) - c.1299T>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH09575972 | 438 | N>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8543548A>T Codon: AAC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543548A>T Locations: - p.Asn438Ile (EnsemblPlants:AT4G14940.1) - c.1313A>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8543572_A_T | 446 | K>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8543572A>T Codon: AAG/ATG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543572A>T Locations: - p.Lys446Met (EnsemblPlants:AT4G14940.1) - c.1337A>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00505735 | 484 | E>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8543687A>C Codon: GAA/GAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543687A>C Locations: - p.Glu484Asp (EnsemblPlants:AT4G14940.1) - c.1452A>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8543698_C_T | 488 | T>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 4:g.8543698C>T Codon: ACG/ATG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543698C>T Locations: - p.Thr488Met (EnsemblPlants:AT4G14940.1) - c.1463C>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14196685 | 488 | T>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.2) Somatic: No Accession: 4:g.8543697A>C Codon: ACG/CCG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543697A>C Locations: - p.Thr488Pro (EnsemblPlants:AT4G14940.1) - c.1462A>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8543775_G_T | 514 | G>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.8543775G>T Codon: GGC/TGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543775G>T Locations: - p.Gly514Cys (EnsemblPlants:AT4G14940.1) - c.1540G>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8543779_C_G | 515 | S>W | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: 4:g.8543779C>G Codon: TCG/TGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543779C>G Locations: - p.Ser515Trp (EnsemblPlants:AT4G14940.1) - c.1544C>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00505736 | 516 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8543783T>G Codon: GAT/GAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543783T>G Locations: - p.Asp516Glu (EnsemblPlants:AT4G14940.1) - c.1548T>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14196686 | 516 | D>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 4:g.8543782A>T Codon: GAT/GTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543782A>T Locations: - p.Asp516Val (EnsemblPlants:AT4G14940.1) - c.1547A>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669166 | 523 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.26) Somatic: No Accession: 4:g.8543802G>A Codon: GTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543802G>A Locations: - p.Val523Ile (EnsemblPlants:AT4G14940.1) - c.1567G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669167 | 528 | K>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.8543817A>G Codon: AAG/GAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543817A>G Locations: - p.Lys528Glu (EnsemblPlants:AT4G14940.1) - c.1582A>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669168 | 532 | G>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8543829G>A Codon: GGA/AGA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543829G>A Locations: - p.Gly532Arg (EnsemblPlants:AT4G14940.1) - c.1594G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00505737 | 534 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.38) Somatic: No Accession: 4:g.8543835A>T Codon: ACA/TCA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543835A>T Locations: - p.Thr534Ser (EnsemblPlants:AT4G14940.1) - c.1600A>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8543865_T_G | 544 | L>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8543865T>G Codon: TTA/GTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543865T>G Locations: - p.Leu544Val (EnsemblPlants:AT4G14940.1) - c.1630T>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00505738 | 545 | Q>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.46) Somatic: No Accession: 4:g.8543869A>C Codon: CAA/CCA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543869A>C Locations: - p.Gln545Pro (EnsemblPlants:AT4G14940.1) - c.1634A>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00505739 | 558 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8543907T>A Codon: TTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543907T>A Locations: - p.Leu558Ile (EnsemblPlants:AT4G14940.1) - c.1672T>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00505739 | 558 | L>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.4) Somatic: No Accession: 4:g.8543907T>G Codon: TTA/GTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543907T>G Locations: - p.Leu558Val (EnsemblPlants:AT4G14940.1) - c.1672T>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11753024 | 567 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.63) Somatic: No Accession: 4:g.8543934G>A Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543934G>A Locations: - p.Val567Ile (EnsemblPlants:AT4G14940.1) - c.1699G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8543998_G_A | 588 | R>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.7) Somatic: No Accession: 4:g.8543998G>A Codon: CGT/CAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8543998G>A Locations: - p.Arg588His (EnsemblPlants:AT4G14940.1) - c.1763G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669171 | 589 | G>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8544000G>A Codon: GGC/AGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544000G>A Locations: - p.Gly589Ser (EnsemblPlants:AT4G14940.1) - c.1765G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669172 | 596 | W>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8544022G>T Codon: TGG/TTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544022G>T Locations: - p.Trp596Leu (EnsemblPlants:AT4G14940.1) - c.1787G>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH11753127 | 600 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8544151C>G Codon: AAC/AAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544151C>G Locations: - p.Asn600Lys (EnsemblPlants:AT4G14940.1) - c.1800C>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8544177_T_C | 609 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8544177T>C Codon: GTG/GCG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544177T>C Locations: - p.Val609Ala (EnsemblPlants:AT4G14940.1) - c.1826T>C (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8544181_G_A | 610 | M>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.8544181G>A Codon: ATG/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544181G>A Locations: - p.Met610Ile (EnsemblPlants:AT4G14940.1) - c.1830G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669176 | 614 | V>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8544192T>A Codon: GTT/GAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544192T>A Locations: - p.Val614Asp (EnsemblPlants:AT4G14940.1) - c.1841T>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14196692 | 633 | G>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.86) Somatic: No Accession: 4:g.8544248G>A Codon: GGT/AGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544248G>A Locations: - p.Gly633Ser (EnsemblPlants:AT4G14940.1) - c.1897G>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8544251_G_T | 634 | G>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.8544251G>T Codon: GGT/TGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544251G>T Locations: - p.Gly634Cys (EnsemblPlants:AT4G14940.1) - c.1900G>T (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8544283_T_A | 644 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.8544283T>A Codon: GAT/GAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544283T>A Locations: - p.Asp644Glu (EnsemblPlants:AT4G14940.1) - c.1932T>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
tmp_4_8544286_C_G | 645 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.37) Somatic: No Accession: 4:g.8544286C>G Codon: AAC/AAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544286C>G Locations: - p.Asn645Lys (EnsemblPlants:AT4G14940.1) - c.1935C>G (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06669178 | 648 | L>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 4:g.8544293T>A Codon: TTG/ATG Consequence type: missense Cytogenetic band: Genomic location: 4:g.8544293T>A Locations: - p.Leu648Met (EnsemblPlants:AT4G14940.1) - c.1942T>A (EnsemblPlants:AT4G14940.1) Source type: large scale study Cross-references: |