Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs772732981
- Species
- Homo sapiens
- Symbol
- rs772732981
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RUFY2
- Location
- 10:68404730
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)10:68404730T>C
- HGVS.c name
- ENSEMBL:ENST00000342616.4:n.207A>G
- ENSEMBL:ENST00000388768.6:c.224A>G
- HGVS.p name
- ENSP00000373420:p.Tyr75Cys
- ENSP00000382151:p.Tyr40Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:68341107...68407294 (66.19 kb)
- Assembly version
- Not Available
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