Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs762065487
- Species
- Homo sapiens
- Symbol
- rs762065487
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RUFY2
- Location
- 10:68406780
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000010.11:g.68406780C>A
- HGVS.c name
- ENSEMBL:ENST00000342616.4:n.92+406G>T
- ENSEMBL:ENST00000388768.6:c.83G>T
- HGVS.p name
- ENSP00000373420:p.Arg28Leu
- XP_047281412:p.Arg28Leu
- 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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