Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.44375168C>T | CA1543137049 | FGF10 | c.325+13190G>A (n.325+13190G>A) | dbSNP |
5 | g.44375168C>G | CA118168754 | FGF10 | c.325+13190G>C (n.325+13190G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.44375168C>A | CA1543137050 | FGF10 | c.325+13190G>T (n.325+13190G>T) | dbSNP |