Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.121334711A>G | CA12519585 | WNT16 | c.633+2747A>G (n.633+2747A>G) c.603+2747A>G (n.603+2747A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.121334711A>C | CA832440271 | WNT16 | c.633+2747A>C (n.633+2747A>C) c.603+2747A>C (n.603+2747A>C) | dbSNP gnomAD v3 gnomAD v4 |