Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs775249776
- Species
- Homo sapiens
- Symbol
- rs775249776
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KIF6
- Location
- 6:39431090
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.39431090C>T
- HGVS.c name
- ENSEMBL:ENST00000229913.9:c.70G>A
- ENSEMBL:ENST00000287152.12:c.1717G>A
- HGVS.p name
- ENSP00000229913:p.Val24Ile
- ENSP00000287152:p.Val573Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:39329990...39725408 (395.42 kb)
- Assembly version
- Not Available
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