Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs200875806
- Species
- Homo sapiens
- Symbol
- rs200875806
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TEN1
- Location
- 17:75991577
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- splice region variant&synonymous variant
- HGVS.g name
- NC_000017.11:g.75991577G>A
- HGVS.c name
- ENSEMBL:ENST00000397640.6:c.204G>A
- ENSEMBL:ENST00000567351.5:n.491G>A
- HGVS.p name
- ENSP00000380762:p.Gln68=
- ENSP00000465866:p.Gln68=
- 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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