Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs991922432
- Species
- Homo sapiens
- Symbol
- rs991922432
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CAMK4
- Location
- 5:111224604
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:111224604G>T
- HGVS.c name
- ENSEMBL:ENST00000282356.9:c.121G>T
- ENSEMBL:ENST00000504090.1:n.141G>T
- HGVS.p name
- ENSP00000282356:p.Ala41Ser
- ENSP00000422634:p.Ala41Ser
- 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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