Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs961642913
- Species
- Homo sapiens
- Symbol
- rs961642913
- Category
- Variant
- Variant type
- SNP
- Overlaps
- COX20
- Location
- 1:244835736
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:244835736G>A
- HGVS.c name
- ENSEMBL:ENST00000366528.3:c.22G>A
- ENSEMBL:ENST00000391839.6:n.81G>A
- HGVS.p name
- ENSP00000355486:p.Gly8Ser
- ENSP00000406327:p.Gly8Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:244835306...244845063 (9.76 kb)
- Assembly version
- Not Available
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