Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs759791177
- Species
- Homo sapiens
- Symbol
- rs759791177
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RSPRY1
- Location
- 16:57227380
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000016.10:g.57227380G>A
- HGVS.c name
- ENSEMBL:ENST00000394420.9:c.1200G>A
- ENSEMBL:ENST00000537866.5:c.1200G>A
- HGVS.p name
- ENSP00000377942:p.Ala400=
- ENSP00000443176:p.Ala400=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:57186137...57240469 (54.33 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction