Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs543914514
- Species
- Homo sapiens
- Symbol
- rs543914514
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TEN1
- Location
- 17:75979259
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- (GRCh38)17:75979259A>T
- HGVS.c name
- ENSEMBL:ENST00000397640.6:c.-259A>T
- ENSEMBL:ENST00000567351.5:n.29A>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:75979240...76000586 (21.35 kb)
- Assembly version
- Not Available
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