Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs978998158
- Species
- Homo sapiens
- Symbol
- rs978998158
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CUEDC2
- Location
- 10:102424662
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000010.11:g.102424662C>T
- HGVS.c name
- ENSEMBL:ENST00000369937.5:c.205G>A
- ENSEMBL:ENST00000477994.1:n.274G>A
- HGVS.p name
- ENSP00000358953:p.Ala69Thr
- NP_076945:p.Ala69Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:102423245...102432584 (9.34 kb)
- Assembly version
- Not Available
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