A0A2R8VKS7 · A0A2R8VKS7_MOUSE
- Proteinsingle-stranded DNA cytosine deaminase
- GeneApobec3
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids
- Protein existenceEvidence at protein level
- Annotation score2/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3406273203 | 2 | D>H | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000081.7:g.79789652G>C Codon: GAC/CAC Consequence type: missense Cytogenetic band: 15q Genomic location: NC_000081.7:g.79789652G>C Locations: - p.Asp2His (Ensembl:ENSMUST00000230135) - c.4G>C (Ensembl:ENSMUST00000230135) Source type: large scale study Cross-references: | |||||||
rs3405447683 | 3 | P>L | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: NC_000081.7:g.79789656C>T Codon: CCG/CTG Consequence type: missense Cytogenetic band: 15q Genomic location: NC_000081.7:g.79789656C>T Locations: - p.Pro3Leu (Ensembl:ENSMUST00000230135) - c.8C>T (Ensembl:ENSMUST00000230135) Source type: large scale study Cross-references: | |||||||
rs3389368433 | 21 | L>F | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.16) Somatic: No Accession: NC_000081.7:g.79789709C>T Codon: CTC/TTC Consequence type: missense Cytogenetic band: 15q Genomic location: NC_000081.7:g.79789709C>T Locations: - p.Leu21Phe (Ensembl:ENSMUST00000230135) - c.61C>T (Ensembl:ENSMUST00000230135) Source type: large scale study Cross-references: | |||||||
rs3389368408 | 25 | H>Q | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.29) Somatic: No Accession: NC_000081.7:g.79789723C>A Codon: CAC/CAA Consequence type: missense Cytogenetic band: 15q Genomic location: NC_000081.7:g.79789723C>A Locations: - p.His25Gln (Ensembl:ENSMUST00000230135) - c.75C>A (Ensembl:ENSMUST00000230135) Source type: large scale study Cross-references: | |||||||
rs3406296718 | 26 | R>G | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000081.7:g.79789724C>G Codon: CGC/GGC Consequence type: missense Cytogenetic band: 15q Genomic location: NC_000081.7:g.79789724C>G Locations: - p.Arg26Gly (Ensembl:ENSMUST00000230135) - c.76C>G (Ensembl:ENSMUST00000230135) Source type: large scale study Cross-references: | |||||||
rs3389374746 | 41 | Q>E | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.57) Somatic: No Accession: NC_000081.7:g.79789769C>G Codon: CAA/GAA Consequence type: missense Cytogenetic band: 15q Genomic location: NC_000081.7:g.79789769C>G Locations: - p.Gln41Glu (Ensembl:ENSMUST00000230135) - c.121C>G (Ensembl:ENSMUST00000230135) Source type: large scale study Cross-references: | |||||||
rs3389380563 | 44 | L>R | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.36) Somatic: No Accession: NC_000081.7:g.79789779T>G Codon: CTC/CGC Consequence type: missense Cytogenetic band: 15q Genomic location: NC_000081.7:g.79789779T>G Locations: - p.Leu44Arg (Ensembl:ENSMUST00000230135) - c.131T>G (Ensembl:ENSMUST00000230135) Source type: large scale study Cross-references: | |||||||
rs3406197955 | 74 | T>I | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000081.7:g.79790609C>T Codon: ACA/ATA Consequence type: missense Cytogenetic band: 15q Genomic location: NC_000081.7:g.79790609C>T Locations: - p.Thr74Ile (Ensembl:ENSMUST00000230135) - c.221C>T (Ensembl:ENSMUST00000230135) Source type: large scale study Cross-references: |