Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs775630795
- Species
- Homo sapiens
- Symbol
- rs775630795
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CD164
- Location
- 6:109382342
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.109382342T>C
- HGVS.c name
- ENSEMBL:ENST00000310786.10:c.37A>G
- ENSEMBL:ENST00000324953.9:c.37A>G
- HGVS.p name
- ENSP00000309376:p.Thr13Ala
- ENSP00000314177:p.Thr13Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:109366514...109382467 (15.95 kb)
- Assembly version
- Not Available
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