Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs144655252
- Species
- Homo sapiens
- Symbol
- rs144655252
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DEPDC7
- Location
- 11:33028606
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)11:33028606T>C
- HGVS.c name
- ENSEMBL:ENST00000241051.8:c.596T>C
- ENSEMBL:ENST00000311388.7:c.569T>C
- HGVS.p name
- ENSP00000241051:p.Ile199Thr
- ENSP00000308971:p.Ile190Thr
- 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