Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.44352242T>C | CA11967891 | FGF10 | c.325+36116A>G (n.325+36116A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.44352242T>G | CA1543117646 | FGF10 | c.325+36116A>C (n.325+36116A>C) | dbSNP |
5 | g.44352242T>A | CA1543117647 | FGF10 | c.325+36116A>T (n.325+36116A>T) | dbSNP |