Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs779274948
- Species
- Homo sapiens
- Symbol
- rs779274948
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ECPAS
- Location
- 9:111372455
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:111372455G>T
- HGVS.c name
- ENSEMBL:ENST00000259335.8:c.5036C>A
- ENSEMBL:ENST00000338205.9:c.4502C>A
- HGVS.p name
- ENSP00000259335:p.Thr1679Asn
- ENSP00000339889:p.Thr1501Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:111360685...111484745 (124.06 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction