Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs373390253
- Species
- Homo sapiens
- Symbol
- rs373390253
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GLTPD2
- Location
- 17:4789926
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:4789926C>T
- HGVS.c name
- ENSEMBL:ENST00000331264.8:c.506C>T
- HGVS.p name
- ENSP00000328070:p.Ala169Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:4788964...4790589 (1.63 kb)
- Assembly version
- Not Available
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