Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs766330962
- Species
- Homo sapiens
- Symbol
- rs766330962
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CNOT7
- Location
- 8:17245139
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)8:17245139G>A
- HGVS.c name
- ENSEMBL:ENST00000361272.9:c.14C>T
- ENSEMBL:ENST00000518021.5:n.292C>T
- HGVS.p name
- ENSP00000355279:p.Thr5Ile
- ENSP00000429079:p.Thr5Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:17224966...17246878 (21.91 kb)
- Assembly version
- Not Available
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