Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1471794219
- Species
- Homo sapiens
- Symbol
- rs1471794219
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FOXK2
- Location
- 17:82586017
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:82586017C>T
- HGVS.c name
- ENSEMBL:ENST00000335255.10:c.1393C>T
- ENSEMBL:ENST00000473637.6:n.1569C>T
- HGVS.p name
- ENSP00000335677:p.Pro465Ser
- NP_004505:p.Pro465Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:82519713...82644662 (124.95 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction