Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs758097328
- Species
- Homo sapiens
- Symbol
- rs758097328
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PGF
- Location
- 14:74948570
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)14:74948570C>A
- HGVS.c name
- ENSEMBL:ENST00000238607.10:c.326G>T
- ENSEMBL:ENST00000405431.2:c.329G>T
- HGVS.p name
- ENSP00000238607:p.Arg109Leu
- ENSP00000385365:p.Arg110Leu
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction