Q9SZ58 · BRAT1_ARATH
- ProteinBrassinosteroid-related acyltransferase 1
- GeneBAT1
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids458 (go to sequence)
- Protein existenceEvidence at transcript level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_4_15441198_A_G | 25 | D>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: 4:g.15441198A>G Codon: GAC/GGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441198A>G Locations: - p.Asp25Gly (EnsemblPlants:AT4G31910.1) - c.74A>G (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06809901 | 31 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.16) Somatic: No Accession: 4:g.15441216C>T Codon: ACT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441216C>T Locations: - p.Thr31Ile (EnsemblPlants:AT4G31910.1) - c.92C>T (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15441268_C_A | 48 | F>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.15441268C>A Codon: TTC/TTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441268C>A Locations: - p.Phe48Leu (EnsemblPlants:AT4G31910.1) - c.144C>A (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15441276_A_T | 51 | N>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: 4:g.15441276A>T Codon: AAT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441276A>T Locations: - p.Asn51Ile (EnsemblPlants:AT4G31910.1) - c.152A>T (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12342192 | 59 | S>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.16) Somatic: No Accession: 4:g.15441300C>A Codon: TCC/TAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441300C>A Locations: - p.Ser59Tyr (EnsemblPlants:AT4G31910.1) - c.176C>A (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15441308_T_G | 62 | S>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.16) Somatic: No Accession: 4:g.15441308T>G Codon: TCC/GCC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441308T>G Locations: - p.Ser62Ala (EnsemblPlants:AT4G31910.1) - c.184T>G (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15441383_G_T | 87 | G>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.05) Somatic: No Accession: 4:g.15441383G>T Codon: GGT/TGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441383G>T Locations: - p.Gly87Cys (EnsemblPlants:AT4G31910.1) - c.259G>T (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06809904 | 88 | G>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.15441387G>A Codon: GGC/GAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441387G>A Locations: - p.Gly88Asp (EnsemblPlants:AT4G31910.1) - c.263G>A (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06809905 | 96 | N>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.15441410A>C Codon: AAC/CAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441410A>C Locations: - p.Asn96His (EnsemblPlants:AT4G31910.1) - c.286A>C (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15441450_G_T | 109 | G>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.28) Somatic: No Accession: 4:g.15441450G>T Codon: GGT/GTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441450G>T Locations: - p.Gly109Val (EnsemblPlants:AT4G31910.1) - c.326G>T (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15441462_C_T | 113 | S>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.15441462C>T Codon: TCC/TTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441462C>T Locations: - p.Ser113Phe (EnsemblPlants:AT4G31910.1) - c.338C>T (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06809906 | 116 | G>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.15441471G>A Codon: GGT/GAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441471G>A Locations: - p.Gly116Asp (EnsemblPlants:AT4G31910.1) - c.347G>A (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15441504_A_G | 127 | N>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: 4:g.15441504A>G Codon: AAT/AGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441504A>G Locations: - p.Asn127Ser (EnsemblPlants:AT4G31910.1) - c.380A>G (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14323449 | 129 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.15441509G>A Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15441509G>A Locations: - p.Val129Ile (EnsemblPlants:AT4G31910.1) - c.385G>A (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15442597_T_A | 151 | F>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.15442597T>A Codon: TTT/TTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15442597T>A Locations: - p.Phe151Leu (EnsemblPlants:AT4G31910.1) - c.453T>A (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15442715_A_G | 191 | S>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.47) Somatic: No Accession: 4:g.15442715A>G Codon: AGC/GGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15442715A>G Locations: - p.Ser191Gly (EnsemblPlants:AT4G31910.1) - c.571A>G (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06809916 | 196 | K>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.51) Somatic: No Accession: 4:g.15442731A>C Codon: AAA/ACA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15442731A>C Locations: - p.Lys196Thr (EnsemblPlants:AT4G31910.1) - c.587A>C (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06809917 | 198 | E>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.81) Somatic: No Accession: 4:g.15442738A>C Codon: GAA/GAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15442738A>C Locations: - p.Glu198Asp (EnsemblPlants:AT4G31910.1) - c.594A>C (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15442778_C_A | 212 | L>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 4:g.15442778C>A Codon: CTG/ATG Consequence type: missense Cytogenetic band: Genomic location: 4:g.15442778C>A Locations: - p.Leu212Met (EnsemblPlants:AT4G31910.1) - c.634C>A (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15442787_C_T | 215 | R>W | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 4:g.15442787C>T Codon: CGG/TGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.15442787C>T Locations: - p.Arg215Trp (EnsemblPlants:AT4G31910.1) - c.643C>T (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00547651 | 218 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.25) Somatic: No Accession: 4:g.15442796G>A Codon: GTC/ATC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15442796G>A Locations: - p.Val218Ile (EnsemblPlants:AT4G31910.1) - c.652G>A (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15442928_A_G | 262 | N>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 4:g.15442928A>G Codon: AAT/GAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15442928A>G Locations: - p.Asn262Asp (EnsemblPlants:AT4G31910.1) - c.784A>G (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06809919 | 271 | K>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.74) Somatic: No Accession: 4:g.15442956A>G Codon: AAG/AGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.15442956A>G Locations: - p.Lys271Arg (EnsemblPlants:AT4G31910.1) - c.812A>G (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15442997_C_G | 285 | L>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.81) Somatic: No Accession: 4:g.15442997C>G Codon: CTT/GTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15442997C>G Locations: - p.Leu285Val (EnsemblPlants:AT4G31910.1) - c.853C>G (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02949438 | 295 | R>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.15443203G>A Codon: AGG/AAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.15443203G>A Locations: - p.Arg295Lys (EnsemblPlants:AT4G31910.1) - c.884G>A (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06809925 | 296 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.15443206C>T Codon: GCT/GTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15443206C>T Locations: - p.Ala296Val (EnsemblPlants:AT4G31910.1) - c.887C>T (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15443229_A_T | 304 | M>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.28) Somatic: No Accession: 4:g.15443229A>T Codon: ATG/TTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.15443229A>T Locations: - p.Met304Leu (EnsemblPlants:AT4G31910.1) - c.910A>T (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12342362 | 349 | E>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.27) Somatic: No Accession: 4:g.15443366G>T Codon: GAG/GAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15443366G>T Locations: - p.Glu349Asp (EnsemblPlants:AT4G31910.1) - c.1047G>T (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15443451_A_C | 378 | N>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: 4:g.15443451A>C Codon: AAT/CAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15443451A>C Locations: - p.Asn378His (EnsemblPlants:AT4G31910.1) - c.1132A>C (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06809932 | 413 | Y>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: 4:g.15443556T>A Codon: TAC/AAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15443556T>A Locations: - p.Tyr413Asn (EnsemblPlants:AT4G31910.1) - c.1237T>A (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06809933 | 425 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: 4:g.15443593C>T Codon: GCT/GTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15443593C>T Locations: - p.Ala425Val (EnsemblPlants:AT4G31910.1) - c.1274C>T (EnsemblPlants:AT4G31910.1) Source type: large scale study Cross-references: |