Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs200888271
- Species
- Homo sapiens
- Symbol
- rs200888271
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PLEKHG4
- Location
- 16:67288488
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- splice acceptor variant
- HGVS.g name
- (GRCh38)16:67288488G>C
- HGVS.c name
- ENSEMBL:ENST00000360461.9:c.3455-1G>C
- ENSEMBL:ENST00000379344.8:c.3455-1G>C
- HGVS.p name
- XP_047289854:p.Ser1156Thr
- XP_047289855:p.Ser963Thr
- 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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