Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1057524315
- Species
- Homo sapiens
- Symbol
- rs1057524315
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CAMTA2
- Location
- 17:4978503
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- splice donor variant
- HGVS.g name
- NC_000017.11:g.4978503C>T
- HGVS.c name
- ENSEMBL:ENST00000348066.8:c.1765+1G>A
- ENSEMBL:ENST00000361571.9:c.1762+1G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:4967992...4987675 (19.68 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction