Q12234 · RUD3_YEAST
- ProteinGRIP domain-containing protein RUD3
- GeneRUD3
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids484 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score4/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
s15-748820 | 54 | A>V | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.19) Somatic: No Accession: XV:g.748819G>A Codon: GCA/GTA Consequence type: missense Cytogenetic band: Genomic location: XV:g.748819G>A Locations: - p.Ala54Val (Ensembl:YOR216C_mRNA) - c.161C>T (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748820 | |||||||
s15-748781 | 67 | V>A | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: XV:g.748780A>G Codon: GTA/GCA Consequence type: missense Cytogenetic band: Genomic location: XV:g.748780A>G Locations: - p.Val67Ala (Ensembl:YOR216C_mRNA) - c.200T>C (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748781 | |||||||
s15-748713 | 90 | G>R | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.31) Somatic: No Accession: XV:g.748712C>G Codon: GGT/CGT Consequence type: missense Cytogenetic band: Genomic location: XV:g.748712C>G Locations: - p.Gly90Arg (Ensembl:YOR216C_mRNA) - c.268G>C (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748713 | |||||||
s15-748699 | 94 | K>N | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.33) Somatic: No Accession: XV:g.748698C>G Codon: AAG/AAC Consequence type: missense Cytogenetic band: Genomic location: XV:g.748698C>G Locations: - p.Lys94Asn (Ensembl:YOR216C_mRNA) - c.282G>C (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748699 | |||||||
s15-748682 | 100 | I>T | SGRP | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: XV:g.748681A>G Codon: ATT/ACT Consequence type: missense Cytogenetic band: Genomic location: XV:g.748681A>G Locations: - p.Ile100Thr (Ensembl:YOR216C_mRNA) - c.299T>C (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748682 | |||||||
s15-748656 | 109 | H>Y | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.05) Somatic: No Accession: XV:g.748655G>A Codon: CAC/TAC Consequence type: missense Cytogenetic band: Genomic location: XV:g.748655G>A Locations: - p.His109Tyr (Ensembl:YOR216C_mRNA) - c.325C>T (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748656 | |||||||
s15-748605 | 126 | N>D | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.41) Somatic: No Accession: XV:g.748604T>C Codon: AAT/GAT Consequence type: missense Cytogenetic band: Genomic location: XV:g.748604T>C Locations: - p.Asn126Asp (Ensembl:YOR216C_mRNA) - c.376A>G (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748605 | |||||||
s15-748350 | 211 | Q>K | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: XV:g.748349G>T Codon: CAA/AAA Consequence type: missense Cytogenetic band: Genomic location: XV:g.748349G>T Locations: - p.Gln211Lys (Ensembl:YOR216C_mRNA) - c.631C>A (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748350 | |||||||
s15-748131 | 284 | A>S | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.73) Somatic: No Accession: XV:g.748130C>A Codon: GCT/TCT Consequence type: missense Cytogenetic band: Genomic location: XV:g.748130C>A Locations: - p.Ala284Ser (Ensembl:YOR216C_mRNA) - c.850G>T (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748131 | |||||||
s15-748050 | 311 | N>D | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.64) Somatic: No Accession: XV:g.748049T>C Codon: AAC/GAC Consequence type: missense Cytogenetic band: Genomic location: XV:g.748049T>C Locations: - p.Asn311Asp (Ensembl:YOR216C_mRNA) - c.931A>G (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748050 | |||||||
s15-748031 | 317 | A>V | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.48) Somatic: No Accession: XV:g.748030G>A Codon: GCT/GTT Consequence type: missense Cytogenetic band: Genomic location: XV:g.748030G>A Locations: - p.Ala317Val (Ensembl:YOR216C_mRNA) - c.950C>T (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748031 | |||||||
s15-748005 | 326 | S>A | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: XV:g.748004A>C Codon: TCT/GCT Consequence type: missense Cytogenetic band: Genomic location: XV:g.748004A>C Locations: - p.Ser326Ala (Ensembl:YOR216C_mRNA) - c.976T>G (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-748005 | |||||||
s15-747921 | 354 | A>T | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.53) Somatic: No Accession: XV:g.747920C>T Codon: GCC/ACC Consequence type: missense Cytogenetic band: Genomic location: XV:g.747920C>T Locations: - p.Ala354Thr (Ensembl:YOR216C_mRNA) - c.1060G>A (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-747921 | |||||||
s15-747905 | 359 | A>V | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: XV:g.747904G>A Codon: GCC/GTC Consequence type: missense Cytogenetic band: Genomic location: XV:g.747904G>A Locations: - p.Ala359Val (Ensembl:YOR216C_mRNA) - c.1076C>T (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-747905 | |||||||
s15-747867 | 372 | H>Y | SGRP | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: XV:g.747866G>A Codon: CAC/TAC Consequence type: missense Cytogenetic band: Genomic location: XV:g.747866G>A Locations: - p.His372Tyr (Ensembl:YOR216C_mRNA) - c.1114C>T (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-747867 | |||||||
s15-747613 | 456 | E>D | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.57) Somatic: No Accession: XV:g.747612C>G Codon: GAG/GAC Consequence type: missense Cytogenetic band: Genomic location: XV:g.747612C>G Locations: - p.Glu456Asp (Ensembl:YOR216C_mRNA) - c.1368G>C (Ensembl:YOR216C_mRNA) Source type: large scale study Cross-references: - SGRP: s15-747613 |