Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.69819192G>A | CA1980747152 | FGF3 | c.-259C>T (n.-259C>T) n.86+119G>A | dbSNP |
11 | g.69819192G>C | CA223501279 | FGF3 | c.-259C>G (n.-259C>G) n.86+119G>C | dbSNP |
11 | g.69819192G= | CA1980747151 | FGF3 | c.-259C= (n.-259C=) n.86+119G= | dbSNP |