Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1431907802
- Species
- Homo sapiens
- Symbol
- rs1431907802
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2F5
- Location
- 8:85209379
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)8:85209379C>A
- HGVS.c name
- ENSEMBL:ENST00000256117.9:n.662C>A
- ENSEMBL:ENST00000416274.7:c.853C>A
- HGVS.p name
- ENSP00000398124:p.Gln285Lys
- ENSP00000414312:p.Gln285Lys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:85177154...85217158 (40.00 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction