Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs369417903
- Species
- Homo sapiens
- Symbol
- rs369417903
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ANO10
- Location
- 3:43577122
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000003.12:g.43577122C>T
- HGVS.c name
- ENSEMBL:ENST00000292246.8:c.732G>A
- ENSEMBL:ENST00000350459.8:c.593-2258G>A
- HGVS.p name
- ENSP00000292246:p.Val244=
- ENSP00000379398:p.Val178=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:43354859...43691594 (336.74 kb)
- Assembly version
- Not Available
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