Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs962406905
- Species
- Homo sapiens
- Symbol
- rs962406905
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRK1
- Location
- 15:100973986
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000015.10:g.100973986C>T
- HGVS.c name
- ENSEMBL:ENST00000388948.8:c.261+19C>T
- ENSEMBL:ENST00000527698.1:n.517C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:100919327...101078257 (158.93 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction