Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs775165370
- Species
- Homo sapiens
- Symbol
- rs775165370
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HLTF
- Location
- 3:149039066
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.149039066C>A
- HGVS.c name
- ENSEMBL:ENST00000310053.10:c.2779G>T
- ENSEMBL:ENST00000392912.6:c.2779G>T
- HGVS.p name
- ENSP00000308944:p.Val927Leu
- ENSP00000376644:p.Val927Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:149030063...149086554 (56.49 kb)
- Assembly version
- Not Available
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