Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs150103724
- Species
- Homo sapiens
- Symbol
- rs150103724
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BTBD7
- Location
- 14:93248648
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000014.9:g.93248648C>T
- HGVS.c name
- ENSEMBL:ENST00000334746.10:c.1949G>A
- ENSEMBL:ENST00000355125.3:n.649G>A
- HGVS.p name
- ENSP00000335615:p.Arg650His
- ENSP00000450778:p.Arg265His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:93237550...93333092 (95.54 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction