Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs771650335
- Species
- Homo sapiens
- Symbol
- rs771650335
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GMDS
- Location
- 6:2117538
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)6:2117538G>A
- HGVS.c name
- ENSEMBL:ENST00000380815.5:c.166C>T
- ENSEMBL:ENST00000530927.5:c.76C>T
- HGVS.p name
- ENSP00000370194:p.Arg56Trp
- ENSP00000436726:p.Arg26Trp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:1623806...2245605 (621.80 kb)
- Assembly version
- Not Available
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