Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1171227939
- Species
- Homo sapiens
- Symbol
- rs1171227939
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FBXO43
- Location
- 8:100141395
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000008.11:g.100141395C>T
- HGVS.c name
- ENSEMBL:ENST00000428847.3:c.859G>A
- ENSEMBL:ENST00000517806.5:n.1568G>A
- HGVS.p name
- ENSP00000403293:p.Val287Ile
- XP_011515292:p.Val253Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:100133351...100150569 (17.22 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction