Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs76665287
- Species
- Homo sapiens
- Symbol
- rs76665287
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BBOF1
- Location
- 14:74058344
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (GRCh38)14:74058344C>T
- HGVS.c name
- ENSEMBL:ENST00000394009.5:c.1578+1086C>T
- ENSEMBL:ENST00000492026.4:n.1379+1086C>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
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