Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1929475941
- Species
- Homo sapiens
- Symbol
- rs1929475941
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LARGE1
- Location
- 22:33277142
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000022.11:g.33277142C>G
- HGVS.c name
- ENSEMBL:ENST00000354992.7:c.1991G>C
- ENSEMBL:ENST00000397394.8:c.1991G>C
- HGVS.p name
- ENSP00000347088:p.Arg664Thr
- ENSP00000380549:p.Arg664Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:33066663...33922841 (856.18 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction