Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs377162968
- Species
- Homo sapiens
- Symbol
- rs377162968
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRK1
- Location
- 15:101010446
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_000015.10:g.101010446G>A
- HGVS.c name
- ENSEMBL:ENST00000388948.8:c.990-4G>A
- RefSeq:NM_024652.6:c.990-4G>A
- 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