Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs112689182
- Species
- Homo sapiens
- Symbol
- rs112689182
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BBOF1
- Location
- 14:74058281
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (GRCh38)14:74058281C>T
- HGVS.c name
- ENSEMBL:ENST00000394009.5:c.1578+1023C>T
- ENSEMBL:ENST00000492026.4:n.1379+1023C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:74019349...74082864 (63.52 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction