Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs207466323
- Species
- Homo sapiens
- Symbol
- rs207466323
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CAMK4
- Location
- 5:111371525
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)5:111371525G>T
- HGVS.c name
- ENSEMBL:ENST00000282356.9:c.241-3325G>T
- ENSEMBL:ENST00000502916.5:n.165-3325G>T
- HGVS.p name
- Not Available
- 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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