Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs367948856
- Species
- Homo sapiens
- Symbol
- rs367948856
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DEPDC7
- Location
- 11:33033398
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000011.10:g.33033398G>T
- HGVS.c name
- ENSEMBL:ENST00000241051.8:c.1479G>T
- ENSEMBL:ENST00000311388.7:c.1452G>T
- HGVS.p name
- ENSP00000241051:p.Leu493Phe
- ENSP00000308971:p.Leu484Phe
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:33015876...33033582 (17.71 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction