Q8BK32 · Q8BK32_MOUSE
- ProteinNuclear receptor corepressor 1
- GeneNcor1
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids291 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score2/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3389166219 | 25 | V>F | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000077.7:g.62329199C>A Codon: GTC/TTC Consequence type: missense Cytogenetic band: 11q Genomic location: NC_000077.7:g.62329199C>A Locations: - p.Val25Phe (Ensembl:ENSMUST00000069456) - c.73G>T (Ensembl:ENSMUST00000069456) Source type: large scale study Cross-references: | |||||||
rs3548710509 | 51 | S>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000077.7:g.62324482C>T Codon: AGC/AAC Consequence type: missense Cytogenetic band: 11q Genomic location: NC_000077.7:g.62324482C>T Locations: - p.Ser51Asn (Ensembl:ENSMUST00000069456) - c.152G>A (Ensembl:ENSMUST00000069456) Source type: large scale study Cross-references: | |||||||
rs26925020 | 55 | Q>K | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000077.7:g.62324471G>T Codon: CAG/AAG Consequence type: missense Cytogenetic band: 11q Genomic location: NC_000077.7:g.62324471G>T Locations: - p.Gln55Lys (Ensembl:ENSMUST00000069456) - c.163C>A (Ensembl:ENSMUST00000069456) Source type: large scale study Cross-references: | |||||||
rs26925021 | 67 | R>L | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000077.7:g.62324434C>A Codon: CGA/CTA Consequence type: missense Cytogenetic band: 11q Genomic location: NC_000077.7:g.62324434C>A Locations: - p.Arg67Leu (Ensembl:ENSMUST00000069456) - c.200G>T (Ensembl:ENSMUST00000069456) Source type: large scale study Cross-references: | |||||||
rs218664265 | 88 | T>I | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.01) Somatic: No Accession: NC_000077.7:g.62313876G>A Codon: ACT/ATT Consequence type: missense Cytogenetic band: 11q Genomic location: NC_000077.7:g.62313876G>A Locations: - p.Thr88Ile (Ensembl:ENSMUST00000069456) - c.263C>T (Ensembl:ENSMUST00000069456) Source type: large scale study Cross-references: | |||||||
rs3389165183 | 117 | D>G | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000077.7:g.62313789T>C Codon: GAT/GGT Consequence type: missense Cytogenetic band: 11q Genomic location: NC_000077.7:g.62313789T>C Locations: - p.Asp117Gly (Ensembl:ENSMUST00000069456) - c.350A>G (Ensembl:ENSMUST00000069456) Source type: large scale study Cross-references: | |||||||
rs3389166276 | 122 | R>H | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000077.7:g.62313774C>T Codon: CGT/CAT Consequence type: missense Cytogenetic band: 11q Genomic location: NC_000077.7:g.62313774C>T Locations: - p.Arg122His (Ensembl:ENSMUST00000069456) - c.365G>A (Ensembl:ENSMUST00000069456) Source type: large scale study Cross-references: | |||||||
rs3389171965 | 145 | K>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000077.7:g.62313704C>A Codon: AAG/AAT Consequence type: missense Cytogenetic band: 11q Genomic location: NC_000077.7:g.62313704C>A Locations: - p.Lys145Asn (Ensembl:ENSMUST00000069456) - c.435G>T (Ensembl:ENSMUST00000069456) Source type: large scale study Cross-references: | |||||||
rs3389161642 | 255 | F>L | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000077.7:g.62295265A>G Codon: TTT/CTT Consequence type: missense Cytogenetic band: 11q Genomic location: NC_000077.7:g.62295265A>G Locations: - p.Phe255Leu (Ensembl:ENSMUST00000069456) - c.763T>C (Ensembl:ENSMUST00000069456) Source type: large scale study Cross-references: |