G3UWG7 · G3UWG7_MOUSE
- ProteinWASH complex subunit 3
- GeneWashc3
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids179 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score2/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3389107829 | 25 | R>G | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.88037695A>G Codon: AGA/GGA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.88037695A>G Locations: - p.Arg25Gly (Ensembl:ENSMUST00000171151) - c.73A>G (Ensembl:ENSMUST00000171151) Source type: large scale study Cross-references: | |||||||
rs3389119510 | 62 | I>S | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.88049543T>G Codon: ATT/AGT Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.88049543T>G Locations: - p.Ile62Ser (Ensembl:ENSMUST00000171151) - c.185T>G (Ensembl:ENSMUST00000171151) Source type: large scale study Cross-references: | |||||||
rs3389121276 | 74 | S>T | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_000076.7:g.88051832T>A Codon: TCA/ACA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.88051832T>A Locations: - p.Ser74Thr (Ensembl:ENSMUST00000171151) - c.220T>A (Ensembl:ENSMUST00000171151) Source type: large scale study Cross-references: | |||||||
rs233130215 | 117 | A>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: NC_000076.7:g.88055137C>T Codon: GCA/GTA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.88055137C>T Locations: - p.Ala117Val (Ensembl:ENSMUST00000171151) - c.350C>T (Ensembl:ENSMUST00000171151) Source type: large scale study Cross-references: | |||||||
rs3389130317 | 123 | P>S | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.37) Somatic: No Accession: NC_000076.7:g.88055154C>T Codon: CCA/TCA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.88055154C>T Locations: - p.Pro123Ser (Ensembl:ENSMUST00000171151) - c.367C>T (Ensembl:ENSMUST00000171151) Source type: large scale study Cross-references: | |||||||
rs3548081238 | 134 | P>L | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000076.7:g.88055188C>T Codon: CCA/CTA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.88055188C>T Locations: - p.Pro134Leu (Ensembl:ENSMUST00000171151) - c.401C>T (Ensembl:ENSMUST00000171151) Source type: large scale study Cross-references: | |||||||
rs3548094450 | 140 | L>R | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.88055206T>G Codon: CTC/CGC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.88055206T>G Locations: - p.Leu140Arg (Ensembl:ENSMUST00000171151) - c.419T>G (Ensembl:ENSMUST00000171151) Source type: large scale study Cross-references: | |||||||
rs48777947 | 162 | P>A | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000076.7:g.88060942C>G Codon: CCC/GCC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.88060942C>G Locations: - p.Pro162Ala (Ensembl:ENSMUST00000171151) - c.484C>G (Ensembl:ENSMUST00000171151) Source type: large scale study Cross-references: |