Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1025369477
- Species
- Homo sapiens
- Symbol
- rs1025369477
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RSPRY1
- Location
- 16:57216945
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000016.10:g.57216945C>T
- HGVS.c name
- ENSEMBL:ENST00000394420.9:c.811C>T
- ENSEMBL:ENST00000537866.5:c.811C>T
- HGVS.p name
- ENSP00000377942:p.Arg271Trp
- ENSP00000443176:p.Arg271Trp
- 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
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