Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs774850626
- Species
- Homo sapiens
- Symbol
- rs774850626
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KIF25
- Location
- 6:168044917
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.168044917G>A
- HGVS.c name
- ENSEMBL:ENST00000354419.6:c.1076G>A
- ENSEMBL:ENST00000443060.6:c.1076G>A
- HGVS.p name
- ENSP00000346401:p.Arg359Gln
- ENSP00000388878:p.Arg359Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:167996241...168045091 (48.85 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction