Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs112697098
- Species
- Homo sapiens
- Symbol
- rs112697098
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRPV2
- Location
- 17:16432161
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000017.11:g.16432161A>G
- HGVS.c name
- ENSEMBL:ENST00000338560.12:c.1850A>G
- ENSEMBL:ENST00000577277.6:c.179-2729A>G
- HGVS.p name
- ENSP00000342222:p.His617Arg
- ENSP00000465609:p.His36Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:16415571...16437003 (21.43 kb)
- Assembly version
- Not Available
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