Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs373078008
- Species
- Homo sapiens
- Symbol
- rs373078008
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRPV2
- Location
- 17:16423711
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:16423711C>T
- HGVS.c name
- ENSEMBL:ENST00000338560.12:c.868C>T
- ENSEMBL:ENST00000455666.1:c.740C>T
- HGVS.p name
- ENSP00000342222:p.Arg290Cys
- ENSP00000390014:p.Pro247Leu
- 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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