Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.8064140delinsGCTTACTTCCC | CA126738 | GATA3 | c.921+2delinsGCTTACTTCCC (n.921+2delinsGCTTACTTCCC) c.924+2delinsGCTTACTTCCC (n.924+2delinsGCTTACTTCCC) n.443+5299delinsGCTTACTTCCC | ClinVar dbSNP |
10 | g.8064140T= | CA1889021541 | GATA3 | c.921+2T= (n.921+2T=) c.924+2T= (n.924+2T=) n.443+5299T= | dbSNP dbSNP |