Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs774856116
- Species
- Homo sapiens
- Symbol
- rs774856116
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KIF25
- Location
- 6:168042611
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)6:168042611C>T
- HGVS.c name
- ENSEMBL:ENST00000354419.6:c.880C>T
- ENSEMBL:ENST00000443060.6:c.880C>T
- HGVS.p name
- ENSP00000346401:p.Arg294Cys
- ENSP00000388878:p.Arg294Cys
- 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
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