Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs969413750
- Species
- Homo sapiens
- Symbol
- rs969413750
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DYNC2LI1
- Location
- 2:43787176
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_000002.12:g.43787176T>C
- HGVS.c name
- ENSEMBL:ENST00000260605.12:c.162-5T>C
- ENSEMBL:ENST00000378587.3:c.113-5T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:43774039...43828347 (54.31 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction