Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.14436619T>C | CA5415013 | FRMD4A,MIR1265 | c.-305+25449A>G (n.-305+25449A>G) c.-82+25449A>G (n.-82+25449A>G) n.44T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.14436619T>G | CA203745940 | FRMD4A,MIR1265 | c.-305+25449A>C (n.-305+25449A>C) c.-82+25449A>C (n.-82+25449A>C) n.44T>G | dbSNP |