Q3ECS3 · BGL35_ARATH
- ProteinMyrosinase 5
- GeneTGG5
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids511 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_1_19087427_G_A | 2 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.09) Somatic: No Accession: 1:g.19087427G>A Codon: GCA/ACA Consequence type: missense Cytogenetic band: Genomic location: 1:g.19087427G>A Locations: - p.Ala2Thr (EnsemblPlants:AT1G51470.1) - c.4G>A (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04933793 | 9 | S>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.72) Somatic: No Accession: 1:g.19087449C>T Codon: TCT/TTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19087449C>T Locations: - p.Ser9Phe (EnsemblPlants:AT1G51470.1) - c.26C>T (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00092780 | 48 | S>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.43) Somatic: No Accession: 1:g.19087566G>C Codon: AGT/ACT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19087566G>C Locations: - p.Ser48Thr (EnsemblPlants:AT1G51470.1) - c.143G>C (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13505242 | 53 | N>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.19087581A>T Codon: AAT/ATT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19087581A>T Locations: - p.Asn53Ile (EnsemblPlants:AT1G51470.1) - c.158A>T (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13505241 | 53 | N>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.19087580A>T Codon: AAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19087580A>T Locations: - p.Asn53Tyr (EnsemblPlants:AT1G51470.1) - c.157A>T (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13505259 | 113 | M>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 1:g.19088076A>C Codon: ATG/CTG Consequence type: missense Cytogenetic band: Genomic location: 1:g.19088076A>C Locations: - p.Met113Leu (EnsemblPlants:AT1G51470.1) - c.337A>C (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
tmp_1_19088331_T_A | 155 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.41) Somatic: No Accession: 1:g.19088331T>A Codon: AAT/AAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.19088331T>A Locations: - p.Asn155Lys (EnsemblPlants:AT1G51470.1) - c.465T>A (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13505269 | 275 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.19089009C>T Codon: ACA/ATA Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089009C>T Locations: - p.Thr275Ile (EnsemblPlants:AT1G51470.1) - c.824C>T (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
tmp_1_19089353_C_T | 343 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.19089353C>T Codon: CTT/TTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089353C>T Locations: - p.Leu343Phe (EnsemblPlants:AT1G51470.1) - c.1027C>T (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
tmp_1_19089407_C_A | 361 | P>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 1:g.19089407C>A Codon: CCT/ACT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089407C>A Locations: - p.Pro361Thr (EnsemblPlants:AT1G51470.1) - c.1081C>A (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14287558 | 382 | S>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 1:g.19089565G>A Codon: AGT/AAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089565G>A Locations: - p.Ser382Asn (EnsemblPlants:AT1G51470.1) - c.1145G>A (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
tmp_1_19089567_C_T | 383 | P>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 1:g.19089567C>T Codon: CCT/TCT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089567C>T Locations: - p.Pro383Ser (EnsemblPlants:AT1G51470.1) - c.1147C>T (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04933815 | 386 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.2) Somatic: No Accession: 1:g.19089576G>A Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089576G>A Locations: - p.Val386Ile (EnsemblPlants:AT1G51470.1) - c.1156G>A (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13505297 | 387 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.19089580T>C Codon: GTG/GCG Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089580T>C Locations: - p.Val387Ala (EnsemblPlants:AT1G51470.1) - c.1160T>C (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14287561 | 390 | S>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.23) Somatic: No Accession: 1:g.19089681G>A Codon: AGC/AAC Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089681G>A Locations: - p.Ser390Asn (EnsemblPlants:AT1G51470.1) - c.1169G>A (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14287561 | 390 | S>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.17) Somatic: No Accession: 1:g.19089681G>C Codon: AGC/ACC Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089681G>C Locations: - p.Ser390Thr (EnsemblPlants:AT1G51470.1) - c.1169G>C (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13505322 | 423 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.19089880G>A Codon: GAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089880G>A Locations: - p.Asp423Asn (EnsemblPlants:AT1G51470.1) - c.1267G>A (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
tmp_1_19089898_G_A | 429 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.15) Somatic: No Accession: 1:g.19089898G>A Codon: GTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089898G>A Locations: - p.Val429Ile (EnsemblPlants:AT1G51470.1) - c.1285G>A (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13505324 | 434 | A>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 1:g.19089914C>G Codon: GCT/GGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089914C>G Locations: - p.Ala434Gly (EnsemblPlants:AT1G51470.1) - c.1301C>G (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13505325 | 439 | G>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.36) Somatic: No Accession: 1:g.19089928G>A Codon: GGA/AGA Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089928G>A Locations: - p.Gly439Arg (EnsemblPlants:AT1G51470.1) - c.1315G>A (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04933830 | 455 | M>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.19089978G>C Codon: ATG/ATC Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089978G>C Locations: - p.Met455Ile (EnsemblPlants:AT1G51470.1) - c.1365G>C (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04933829 | 455 | M>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 1:g.19089976A>T Codon: ATG/TTG Consequence type: missense Cytogenetic band: Genomic location: 1:g.19089976A>T Locations: - p.Met455Leu (EnsemblPlants:AT1G51470.1) - c.1363A>T (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14287600 | 500 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.75) Somatic: No Accession: 1:g.19090210G>A Codon: GCT/ACT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19090210G>A Locations: - p.Ala500Thr (EnsemblPlants:AT1G51470.1) - c.1498G>A (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: | |||||||
tmp_1_19090211_C_T | 500 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.65) Somatic: No Accession: 1:g.19090211C>T Codon: GCT/GTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.19090211C>T Locations: - p.Ala500Val (EnsemblPlants:AT1G51470.1) - c.1499C>T (EnsemblPlants:AT1G51470.1) Source type: large scale study Cross-references: |