Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs752288965
- Species
- Homo sapiens
- Symbol
- rs752288965
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RUFY2
- Location
- 10:68401657
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000010.11:g.68401657C>G
- HGVS.c name
- ENSEMBL:ENST00000342616.4:n.347G>C
- ENSEMBL:ENST00000388768.6:c.364G>C
- HGVS.p name
- ENSP00000373420:p.Glu122Gln
- ENSP00000382151:p.Glu87Gln
- 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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