Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs774625510
- Species
- Homo sapiens
- Symbol
- rs774625510
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GMDS
- Location
- 6:1960938
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)6:1960938G>A
- HGVS.c name
- ENSEMBL:ENST00000380815.5:c.374C>T
- ENSEMBL:ENST00000530459.1:n.127C>T
- HGVS.p name
- ENSP00000370194:p.Ala125Val
- ENSP00000436726:p.Ala95Val
- 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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