Q9C9B0 · U89B1_ARATH
- ProteinFlavonol 3-O-glucosyltransferase UGT89B1
- GeneUGT89B1
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids473 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score4/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
ENSVATH00141873 | 2 | K>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (1) Somatic: No Accession: 1:g.27785147A>C Codon: AAA/ACA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785147A>C Locations: - p.Lys2Thr (EnsemblPlants:AT1G73880.1) - c.5A>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27785171_C_A | 10 | P>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 1:g.27785171C>A Codon: CCG/CAG Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785171C>A Locations: - p.Pro10Gln (EnsemblPlants:AT1G73880.1) - c.29C>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141646 | 12 | K>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.48) Somatic: No Accession: 1:g.27785177A>G Codon: AAG/AGG Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785177A>G Locations: - p.Lys12Arg (EnsemblPlants:AT1G73880.1) - c.35A>G (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141647 | 41 | G>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.78) Somatic: No Accession: 1:g.27785264G>C Codon: GGC/GCC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785264G>C Locations: - p.Gly41Ala (EnsemblPlants:AT1G73880.1) - c.122G>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13804821 | 56 | P>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.27785309C>G Codon: CCT/CGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785309C>G Locations: - p.Pro56Arg (EnsemblPlants:AT1G73880.1) - c.167C>G (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141649 | 66 | V>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.27785338G>T Codon: GTT/TTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785338G>T Locations: - p.Val66Phe (EnsemblPlants:AT1G73880.1) - c.196G>T (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13804822 | 81 | I>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.34) Somatic: No Accession: 1:g.27785383A>C Codon: ATC/CTC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785383A>C Locations: - p.Ile81Leu (EnsemblPlants:AT1G73880.1) - c.241A>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13804823 | 90 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 1:g.27785412C>A Codon: GAC/GAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785412C>A Locations: - p.Asp90Glu (EnsemblPlants:AT1G73880.1) - c.270C>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141652 | 111 | I>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.27785473A>C Codon: ATC/CTC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785473A>C Locations: - p.Ile111Leu (EnsemblPlants:AT1G73880.1) - c.331A>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141654 | 119 | S>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.27785498C>A Codon: TCT/TAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785498C>A Locations: - p.Ser119Tyr (EnsemblPlants:AT1G73880.1) - c.356C>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27785617_A_C | 159 | I>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.36) Somatic: No Accession: 1:g.27785617A>C Codon: ATC/CTC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785617A>C Locations: - p.Ile159Leu (EnsemblPlants:AT1G73880.1) - c.475A>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141658 | 167 | E>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.2) Somatic: No Accession: 1:g.27785642A>G Codon: GAA/GGA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785642A>G Locations: - p.Glu167Gly (EnsemblPlants:AT1G73880.1) - c.500A>G (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141659 | 171 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.92) Somatic: No Accession: 1:g.27785655C>A Codon: AAC/AAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785655C>A Locations: - p.Asn171Lys (EnsemblPlants:AT1G73880.1) - c.513C>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141660 | 175 | H>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.44) Somatic: No Accession: 1:g.27785667C>G Codon: CAC/CAG Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785667C>G Locations: - p.His175Gln (EnsemblPlants:AT1G73880.1) - c.525C>G (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14477574 | 187 | F>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.27785702T>A Codon: TTT/TAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785702T>A Locations: - p.Phe187Tyr (EnsemblPlants:AT1G73880.1) - c.560T>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27785704_G_A | 188 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.43) Somatic: No Accession: 1:g.27785704G>A Codon: GAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785704G>A Locations: - p.Asp188Asn (EnsemblPlants:AT1G73880.1) - c.562G>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14477585 | 224 | S>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.27785813C>T Codon: TCG/TTG Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785813C>T Locations: - p.Ser224Leu (EnsemblPlants:AT1G73880.1) - c.671C>T (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27785884_G_A | 248 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.11) Somatic: No Accession: 1:g.27785884G>A Codon: GTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785884G>A Locations: - p.Val248Ile (EnsemblPlants:AT1G73880.1) - c.742G>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27785888_G_C | 249 | G>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.27785888G>C Codon: GGC/GCC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785888G>C Locations: - p.Gly249Ala (EnsemblPlants:AT1G73880.1) - c.746G>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00141875 | 252 | I>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.27785896A>C Codon: ATT/CTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785896A>C Locations: - p.Ile252Leu (EnsemblPlants:AT1G73880.1) - c.754A>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01533229 | 257 | D>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: 1:g.27785912A>G Codon: GAT/GGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.27785912A>G Locations: - p.Asp257Gly (EnsemblPlants:AT1G73880.1) - c.770A>G (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141661 | 322 | K>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.16) Somatic: No Accession: 1:g.27786107A>T Codon: AAA/ATA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786107A>T Locations: - p.Lys322Ile (EnsemblPlants:AT1G73880.1) - c.965A>T (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01533230 | 323 | D>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.27786109G>T Codon: GAC/TAC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786109G>T Locations: - p.Asp323Tyr (EnsemblPlants:AT1G73880.1) - c.967G>T (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27786136_G_T | 332 | G>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.27786136G>T Codon: GGT/TGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786136G>T Locations: - p.Gly332Cys (EnsemblPlants:AT1G73880.1) - c.994G>T (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27786167_T_A | 342 | L>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.27786167T>A Codon: CTG/CAG Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786167T>A Locations: - p.Leu342Gln (EnsemblPlants:AT1G73880.1) - c.1025T>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14477587 | 359 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: 1:g.27786217G>A Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786217G>A Locations: - p.Val359Ile (EnsemblPlants:AT1G73880.1) - c.1075G>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27786268_G_T | 376 | V>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 1:g.27786268G>T Codon: GTC/TTC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786268G>T Locations: - p.Val376Phe (EnsemblPlants:AT1G73880.1) - c.1126G>T (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27786271_G_T | 377 | A>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.16) Somatic: No Accession: 1:g.27786271G>T Codon: GCC/TCC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786271G>T Locations: - p.Ala377Ser (EnsemblPlants:AT1G73880.1) - c.1129G>T (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141664 | 391 | Y>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.27786314A>T Codon: TAC/TTC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786314A>T Locations: - p.Tyr391Phe (EnsemblPlants:AT1G73880.1) - c.1172A>T (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00141882 | 399 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.87) Somatic: No Accession: 1:g.27786339T>A Codon: GAT/GAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786339T>A Locations: - p.Asp399Glu (EnsemblPlants:AT1G73880.1) - c.1197T>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01533232 | 417 | P>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.27786391C>T Codon: CCG/TCG Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786391C>T Locations: - p.Pro417Ser (EnsemblPlants:AT1G73880.1) - c.1249C>T (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01533234 | 422 | R>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.27786407G>C Codon: CGA/CCA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786407G>C Locations: - p.Arg422Pro (EnsemblPlants:AT1G73880.1) - c.1265G>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13804829 | 426 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.27786420T>A Codon: GAT/GAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786420T>A Locations: - p.Asp426Glu (EnsemblPlants:AT1G73880.1) - c.1278T>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27786430_G_A | 430 | G>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.33) Somatic: No Accession: 1:g.27786430G>A Codon: GGA/AGA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786430G>A Locations: - p.Gly430Arg (EnsemblPlants:AT1G73880.1) - c.1288G>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00141886 | 431 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.78) Somatic: No Accession: 1:g.27786435T>G Codon: AAT/AAG Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786435T>G Locations: - p.Asn431Lys (EnsemblPlants:AT1G73880.1) - c.1293T>G (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141666 | 436 | I>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: 1:g.27786448A>G Codon: ATC/GTC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786448A>G Locations: - p.Ile436Val (EnsemblPlants:AT1G73880.1) - c.1306A>G (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01533236 | 453 | G>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.27786499G>C Codon: GGG/CGG Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786499G>C Locations: - p.Gly453Arg (EnsemblPlants:AT1G73880.1) - c.1357G>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01533239 | 457 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.27786513T>G Codon: AAT/AAG Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786513T>G Locations: - p.Asn457Lys (EnsemblPlants:AT1G73880.1) - c.1371T>G (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27786517_T_A | 459 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 1:g.27786517T>A Codon: TTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786517T>A Locations: - p.Leu459Ile (EnsemblPlants:AT1G73880.1) - c.1375T>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01533240 | 464 | Q>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.27786532C>A Codon: CAA/AAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786532C>A Locations: - p.Gln464Lys (EnsemblPlants:AT1G73880.1) - c.1390C>A (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01533241 | 464 | Q>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.33) Somatic: No Accession: 1:g.27786533A>G Codon: CAA/CGA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786533A>G Locations: - p.Gln464Arg (EnsemblPlants:AT1G73880.1) - c.1391A>G (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05141668 | 466 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.27786539T>C Codon: GTC/GCC Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786539T>C Locations: - p.Val466Ala (EnsemblPlants:AT1G73880.1) - c.1397T>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27786544_A_C | 468 | S>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.18) Somatic: No Accession: 1:g.27786544A>C Codon: AGT/CGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786544A>C Locations: - p.Ser468Arg (EnsemblPlants:AT1G73880.1) - c.1402A>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: | |||||||
tmp_1_27786560_A_C | 473 | K>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.05) Somatic: No Accession: 1:g.27786560A>C Codon: AAA/ACA Consequence type: missense Cytogenetic band: Genomic location: 1:g.27786560A>C Locations: - p.Lys473Thr (EnsemblPlants:AT1G73880.1) - c.1418A>C (EnsemblPlants:AT1G73880.1) Source type: large scale study Cross-references: |