Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1269922798
- Species
- Homo sapiens
- Symbol
- rs1269922798
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CDC20B
- Location
- 5:55160289
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:55160289T>C
- HGVS.c name
- ENSEMBL:ENST00000296733.5:c.126+12299A>G
- ENSEMBL:ENST00000296734.6:c.97T>C
- HGVS.p name
- ENSP00000296734:p.Phe33Leu
- ENSP00000423822:p.Phe33Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:55112971...55173177 (60.21 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction