Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1033685337
- Species
- Homo sapiens
- Symbol
- rs1033685337
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRK1
- Location
- 15:100989243
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_000015.10:g.100989243C>T
- HGVS.c name
- ENSEMBL:ENST00000388948.8:c.614-7C>T
- ENSEMBL:ENST00000525284.5:n.644-7C>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
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