Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs779010896
- Species
- Homo sapiens
- Symbol
- rs779010896
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NOXRED1
- Location
- 14:77405937
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000014.9:g.77405937T>C
- HGVS.c name
- ENSEMBL:ENST00000380835.7:c.881A>G
- ENSEMBL:ENST00000555901.1:n.1636A>G
- HGVS.p name
- ENSP00000370215:p.Tyr294Cys
- XP_011534730:p.Tyr294Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:77394021...77426013 (31.99 kb)
- Assembly version
- Not Available
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