Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1346126712
- Species
- Homo sapiens
- Symbol
- rs1346126712
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NOL6
- Location
- 9:33466105
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:33466105C>A
- HGVS.c name
- ENSEMBL:ENST00000297990.9:c.2330G>T
- ENSEMBL:ENST00000353159.6:c.1950+807G>T
- HGVS.p name
- ENSP00000297990:p.Cys777Phe
- ENSP00000368784:p.Cys777Phe
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:33461353...33473930 (12.58 kb)
- Assembly version
- Not Available
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