Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs758131541
- Species
- Homo sapiens
- Symbol
- rs758131541
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRK1
- Location
- 15:101024881
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)15:101024881G>T
- HGVS.c name
- ENSEMBL:ENST00000388948.8:c.2146G>T
- ENSEMBL:ENST00000525284.5:n.2179G>T
- HGVS.p name
- ENSP00000373600:p.Asp716Tyr
- NP_078928:p.Asp716Tyr
- 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