Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs144622202
- Species
- Homo sapiens
- Symbol
- rs144622202
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DESI1
- Location
- 22:41601108
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)22:41601108C>T
- HGVS.c name
- ENSEMBL:ENST00000263256.7:c.496G>A
- ENSEMBL:ENST00000468151.1:n.183G>A
- HGVS.p name
- ENSP00000263256:p.Gly166Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:41598028...41621043 (23.02 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction