Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs553559355
- Species
- Homo sapiens
- Symbol
- rs553559355
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FBXO43
- Location
- 8:100141935
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000008.11:g.100141935G>A
- HGVS.c name
- ENSEMBL:ENST00000428847.3:c.319C>T
- ENSEMBL:ENST00000517806.5:n.1028C>T
- HGVS.p name
- ENSP00000403293:p.His107Tyr
- NP_001025031:p.His107Tyr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:100133351...100150569 (17.22 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction