Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs146759585
- Species
- Homo sapiens
- Symbol
- rs146759585
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CDO1
- Location
- 5:115806456
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:115806456A>T
- HGVS.c name
- ENSEMBL:ENST00000250535.5:c.466T>A
- ENSEMBL:ENST00000502631.1:n.446T>A
- HGVS.p name
- ENSP00000250535:p.Leu156Met
- NP_001310494:p.Leu175Met
- 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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