Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs117692271
- Species
- Homo sapiens
- Symbol
- rs117692271
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FOXK2
- Location
- 17:82571738
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)17:82571738G>T
- HGVS.c name
- ENSEMBL:ENST00000335255.10:c.777G>T
- ENSEMBL:ENST00000473637.6:n.953G>T
- HGVS.p name
- ENSP00000335677:p.Pro259=
- ENSP00000432663:p.Pro139=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:82519713...82644662 (124.95 kb)
- Assembly version
- Not Available
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