Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1808502366
- Species
- Homo sapiens
- Symbol
- rs1808502366
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CNOT7
- Location
- 8:17230748
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)8:17230748T>C
- HGVS.c name
- ENSEMBL:ENST00000361272.9:c.830A>G
- ENSEMBL:ENST00000518541.5:c.246A>G
- HGVS.p name
- ENSP00000355279:p.Tyr277Cys
- ENSP00000430263:p.Ile82Met
- 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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