Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1406556113
- Species
- Homo sapiens
- Symbol
- rs1406556113
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CAMK4
- Location
- 5:111224572
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:111224572C>G
- HGVS.c name
- ENSEMBL:ENST00000282356.9:c.89C>G
- ENSEMBL:ENST00000504090.1:n.109C>G
- HGVS.p name
- ENSP00000282356:p.Pro30Arg
- ENSP00000422634:p.Pro30Arg
- 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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