Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1177513961
- Species
- Homo sapiens
- Symbol
- rs1177513961
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CDO1
- Location
- 5:115816247
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:115816247C>A
- HGVS.c name
- ENSEMBL:ENST00000250535.5:c.151G>T
- ENSEMBL:ENST00000502631.1:n.74+337G>T
- HGVS.p name
- ENSP00000250535:p.Ala51Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:115804733...115816659 (11.93 kb)
- Assembly version
- Not Available
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