Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs369151536
- Species
- Homo sapiens
- Symbol
- rs369151536
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PLEKHG4
- Location
- 16:67284771
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)16:67284771C>T
- HGVS.c name
- ENSEMBL:ENST00000360461.9:c.1751C>T
- ENSEMBL:ENST00000379344.8:c.1751C>T
- HGVS.p name
- ENSP00000353646:p.Pro584Leu
- ENSP00000368649:p.Pro584Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:67277510...67289499 (11.99 kb)
- Assembly version
- Not Available
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