Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs143979132
- Species
- Homo sapiens
- Symbol
- rs143979132
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CAMK4
- Location
- 5:111484371
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000005.10:g.111484371A>G
- HGVS.c name
- ENSEMBL:ENST00000282356.9:c.1327A>G
- ENSEMBL:ENST00000509645.1:n.1336A>G
- HGVS.p name
- ENSP00000282356:p.Thr443Ala
- ENSP00000422634:p.Thr443Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:111223583...111494886 (271.30 kb)
- Assembly version
- Not Available
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