Q93ZI4 · BGL10_ARATH
- ProteinBeta-glucosidase 10
- GeneBGLU10
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids508 (go to sequence)
- Protein existenceEvidence at transcript level
- Annotation score3/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_4_13864474_G_T | 6 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 4:g.13864474G>T Codon: CTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.13864474G>T Locations: - p.Leu6Ile (EnsemblPlants:AT4G27830.1) - c.16C>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00541886 | 20 | S>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.18) Somatic: No Accession: 4:g.13864431C>T Codon: AGT/AAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.13864431C>T Locations: - p.Ser20Asn (EnsemblPlants:AT4G27830.1) - c.59G>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12266761 | 26 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.43) Somatic: No Accession: 4:g.13864412G>C Codon: AAC/AAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.13864412G>C Locations: - p.Asn26Lys (EnsemblPlants:AT4G27830.1) - c.78C>G (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787451 | 27 | N>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 4:g.13864410T>C Codon: AAT/AGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.13864410T>C Locations: - p.Asn27Ser (EnsemblPlants:AT4G27830.1) - c.80A>G (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787446 | 62 | H>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.13864205T>C Codon: CAC/CGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.13864205T>C Locations: - p.His62Arg (EnsemblPlants:AT4G27830.1) - c.185A>G (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH08369083 | 91 | E>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 4:g.13863818C>T Codon: GAA/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863818C>T Locations: - p.Glu91Lys (EnsemblPlants:AT4G27830.1) - c.271G>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
tmp_4_13863802_G_T | 96 | S>* | 1000Genomes | ||||
Consequence: stop gained Somatic: No Accession: 4:g.13863802G>T Codon: TCA/TAA Consequence type: stop gained Cytogenetic band: Genomic location: 4:g.13863802G>T Locations: - p.Ser96Ter (EnsemblPlants:AT4G27830.1) - c.287C>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787439 | 107 | I>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.13863769A>G Codon: ATA/ACA Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863769A>G Locations: - p.Ile107Thr (EnsemblPlants:AT4G27830.1) - c.320T>C (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787438 | 109 | N>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.13863673T>G Codon: AAT/ACT Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863673T>G Locations: - p.Asn109Thr (EnsemblPlants:AT4G27830.1) - c.326A>C (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
tmp_4_13863517_T_G | 135 | E>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.13863517T>G Codon: GAA/GAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863517T>G Locations: - p.Glu135Asp (EnsemblPlants:AT4G27830.1) - c.405A>C (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
tmp_4_13863466_C_G | 152 | E>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 4:g.13863466C>G Codon: GAG/GAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863466C>G Locations: - p.Glu152Asp (EnsemblPlants:AT4G27830.1) - c.456G>C (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787432 | 199 | Q>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.7) Somatic: No Accession: 4:g.13863231G>C Codon: CAA/GAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863231G>C Locations: - p.Gln199Glu (EnsemblPlants:AT4G27830.1) - c.595C>G (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH08369074 | 201 | I>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.23) Somatic: No Accession: 4:g.13863224A>G Codon: ATC/ACC Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863224A>G Locations: - p.Ile201Thr (EnsemblPlants:AT4G27830.1) - c.602T>C (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH08369073 | 202 | S>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 4:g.13863222A>C Codon: TCG/GCG Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863222A>C Locations: - p.Ser202Ala (EnsemblPlants:AT4G27830.1) - c.604T>G (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
tmp_4_13863196_G_T | 210 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.29) Somatic: No Accession: 4:g.13863196G>T Codon: AAC/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863196G>T Locations: - p.Asn210Lys (EnsemblPlants:AT4G27830.1) - c.630C>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
tmp_4_13863189_T_C | 213 | I>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.56) Somatic: No Accession: 4:g.13863189T>C Codon: ATC/GTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863189T>C Locations: - p.Ile213Val (EnsemblPlants:AT4G27830.1) - c.637A>G (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
tmp_4_13863176_C_G | 217 | S>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.6) Somatic: No Accession: 4:g.13863176C>G Codon: AGT/ACT Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863176C>G Locations: - p.Ser217Thr (EnsemblPlants:AT4G27830.1) - c.650G>C (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787429 | 226 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.13863150G>T Codon: CTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863150G>T Locations: - p.Leu226Ile (EnsemblPlants:AT4G27830.1) - c.676C>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH09501215 | 238 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.11) Somatic: No Accession: 4:g.13863114C>T Codon: GCT/ACT Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863114C>T Locations: - p.Ala238Thr (EnsemblPlants:AT4G27830.1) - c.712G>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02932995 | 249 | T>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.13863011G>T Codon: ACG/AAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.13863011G>T Locations: - p.Thr249Lys (EnsemblPlants:AT4G27830.1) - c.746C>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12266704 | 293 | F>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 4:g.13862800A>C Codon: TTT/TTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.13862800A>C Locations: - p.Phe293Leu (EnsemblPlants:AT4G27830.1) - c.879T>G (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787417 | 306 | S>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 4:g.13862762G>A Codon: TCG/TTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.13862762G>A Locations: - p.Ser306Leu (EnsemblPlants:AT4G27830.1) - c.917C>T (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787416 | 319 | L>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.13862724G>C Codon: CTT/GTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.13862724G>C Locations: - p.Leu319Val (EnsemblPlants:AT4G27830.1) - c.955C>G (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00541883 | 350 | E>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.25) Somatic: No Accession: 4:g.13862631C>T Codon: GAA/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.13862631C>T Locations: - p.Glu350Lys (EnsemblPlants:AT4G27830.1) - c.1048G>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00541882 | 364 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.55) Somatic: No Accession: 4:g.13862503C>T Codon: GCG/ACG Consequence type: missense Cytogenetic band: Genomic location: 4:g.13862503C>T Locations: - p.Ala364Thr (EnsemblPlants:AT4G27830.1) - c.1090G>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787411 | 370 | L>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.29) Somatic: No Accession: 4:g.13862485G>C Codon: CTG/GTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.13862485G>C Locations: - p.Leu370Val (EnsemblPlants:AT4G27830.1) - c.1108C>G (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787405 | 380 | G>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.78) Somatic: No Accession: 4:g.13862377C>T Codon: GGT/AGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.13862377C>T Locations: - p.Gly380Ser (EnsemblPlants:AT4G27830.1) - c.1138G>A (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06787402 | 406 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.14) Somatic: No Accession: 4:g.13862187G>C Codon: GAC/GAG Consequence type: missense Cytogenetic band: Genomic location: 4:g.13862187G>C Locations: - p.Asp406Glu (EnsemblPlants:AT4G27830.1) - c.1218C>G (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12266696 | 407 | S>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.17) Somatic: No Accession: 4:g.13862185G>A Codon: TCG/TTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.13862185G>A Locations: - p.Ser407Leu (EnsemblPlants:AT4G27830.1) - c.1220C>T (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: | |||||||
ENSVATH08369059 | 492 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.13861847T>A Codon: ACT/TCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.13861847T>A Locations: - p.Thr492Ser (EnsemblPlants:AT4G27830.1) - c.1474A>T (EnsemblPlants:AT4G27830.1) Source type: large scale study Cross-references: |