Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs767883960
- Species
- Homo sapiens
- Symbol
- rs767883960
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EFL1
- Location
- 15:82240485
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000015.10:g.82240485C>T
- HGVS.c name
- ENSEMBL:ENST00000268206.12:c.449G>A
- ENSEMBL:ENST00000359445.8:c.296G>A
- HGVS.p name
- ENSP00000268206:p.Arg150His
- ENSP00000352418:p.Arg99His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:82130206...82262773 (132.57 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction