Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs372000874
- Species
- Homo sapiens
- Symbol
- rs372000874
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PGF
- Location
- 14:74949491
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000014.9:g.74949491C>T
- HGVS.c name
- ENSEMBL:ENST00000238607.10:c.178G>A
- ENSEMBL:ENST00000405431.2:c.181G>A
- HGVS.p name
- ENSP00000238607:p.Val60Ile
- ENSP00000385365:p.Val61Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:74941830...74955764 (13.93 kb)
- Assembly version
- Not Available
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