Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs539071080
- Species
- Homo sapiens
- Symbol
- rs539071080
- Category
- Variant
- Variant type
- SNP
- Overlaps
- VIPAS39
- Location
- 14:77448511
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000014.9:g.77448511G>A
- HGVS.c name
- ENSEMBL:ENST00000448935.6:c.340C>T
- ENSEMBL:ENST00000553691.5:n.377C>T
- HGVS.p name
- ENSP00000404815:p.Arg114Cys
- ENSP00000451857:p.Arg189Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:77426675...77457952 (31.28 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction