Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs778010912
- Species
- Homo sapiens
- Symbol
- rs778010912
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DESI2
- Location
- 1:244705727
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.244705727G>A
- HGVS.c name
- ENSEMBL:ENST00000263831.11:c.424G>A
- ENSEMBL:ENST00000302550.16:c.523G>A
- HGVS.p name
- ENSP00000263831:p.Ala142Thr
- ENSP00000306528:p.Ala175Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:244653103...244709033 (55.93 kb)
- Assembly version
- Not Available
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