Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs775083191
- Species
- Homo sapiens
- Symbol
- rs775083191
- Category
- Variant
- Variant type
- SNP
- Overlaps
- STT3B
- Location
- 3:31579950
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:31579950A>G
- HGVS.c name
- ENSEMBL:ENST00000295770.4:c.565A>G
- ENSEMBL:ENST00000423527.5:n.592A>G
- HGVS.p name
- :p.Thr43Ala
- ENSP00000295770:p.Thr189Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:31532638...31638548 (105.91 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction