Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.12517293G>A | CA13702364 | DUSP16 | c.367+2569C>T (n.367+2569C>T) c.87+2569C>T (n.87+2569C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.12517293G>T | CA2016939538 | DUSP16 | c.367+2569C>A (n.367+2569C>A) c.87+2569C>A (n.87+2569C>A) | dbSNP |