P62334 · PRS10_MOUSE
- Protein26S proteasome regulatory subunit 10B
- GenePsmc6
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids389 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score4/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3389276294 | 104 | T>R | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000080.7:g.45572162C>G Codon: ACA/AGA Consequence type: missense Cytogenetic band: 14q Genomic location: NC_000080.7:g.45572162C>G Locations: - p.Thr104Arg (Ensembl:ENSMUST00000022380) - c.311C>G (Ensembl:ENSMUST00000022380) Source type: large scale study Cross-references: | |||||||
rs3389321287 | 140 | E>A | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000080.7:g.45572466A>C Codon: GAA/GCA Consequence type: missense Cytogenetic band: 14q Genomic location: NC_000080.7:g.45572466A>C Locations: - p.Glu140Ala (Ensembl:ENSMUST00000022380) - c.419A>C (Ensembl:ENSMUST00000022380) Source type: large scale study Cross-references: | |||||||
rs3389317630 | 190 | Q>K | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.01) Somatic: No Accession: NC_000080.7:g.45578125C>A Codon: CAG/AAG Consequence type: missense Cytogenetic band: 14q Genomic location: NC_000080.7:g.45578125C>A Locations: - p.Gln190Lys (Ensembl:ENSMUST00000022380) - c.568C>A (Ensembl:ENSMUST00000022380) Source type: large scale study Cross-references: | |||||||
rs3389338182 | 218 | M>L | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000080.7:g.45578290A>T Codon: ATG/TTG Consequence type: missense Cytogenetic band: 14q Genomic location: NC_000080.7:g.45578290A>T Locations: - p.Met218Leu (Ensembl:ENSMUST00000022380) - c.652A>T (Ensembl:ENSMUST00000022380) Source type: large scale study Cross-references: | |||||||
rs3389286501 | 220 | N>D | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.11) Somatic: No Accession: NC_000080.7:g.45578296A>G Codon: AAT/GAT Consequence type: missense Cytogenetic band: 14q Genomic location: NC_000080.7:g.45578296A>G Locations: - p.Asn220Asp (Ensembl:ENSMUST00000022380) - c.658A>G (Ensembl:ENSMUST00000022380) Source type: large scale study Cross-references: | |||||||
rs3389321761 | 223 | R>W | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000080.7:g.45578305A>T Codon: AGG/TGG Consequence type: missense Cytogenetic band: 14q Genomic location: NC_000080.7:g.45578305A>T Locations: - p.Arg223Trp (Ensembl:ENSMUST00000022380) - c.667A>T (Ensembl:ENSMUST00000022380) Source type: large scale study Cross-references: | |||||||
rs3389332867 | 237 | A>D | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000080.7:g.45578348C>A Codon: GCT/GAT Consequence type: missense Cytogenetic band: 14q Genomic location: NC_000080.7:g.45578348C>A Locations: - p.Ala237Asp (Ensembl:ENSMUST00000022380) - c.710C>A (Ensembl:ENSMUST00000022380) Source type: large scale study Cross-references: | |||||||
rs3389286428 | 256 | T>S | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.02) Somatic: No Accession: NC_000080.7:g.45578790C>G Codon: ACT/AGT Consequence type: missense Cytogenetic band: 14q Genomic location: NC_000080.7:g.45578790C>G Locations: - p.Thr256Ser (Ensembl:ENSMUST00000022380) - c.767C>G (Ensembl:ENSMUST00000022380) Source type: large scale study Cross-references: |