Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs562726580
- Species
- Homo sapiens
- Symbol
- rs562726580
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRK1
- Location
- 15:101024941
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)15:101024941C>G
- HGVS.c name
- ENSEMBL:ENST00000388948.8:c.2206C>G
- ENSEMBL:ENST00000525617.2:n.606C>G
- HGVS.p name
- ENSP00000373600:p.Leu736Val
- NP_078928:p.Leu736Val
- 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
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