Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32319080_32319081insTTTTTTT | CA915946926 | BRCA2 | c.71_72insTTTTTTT (p.Leu24PhefsTer9) c.-299_-298insTTTTTTT (n.-299_-298insTTTTTTT) n.191+2553_191+2554insTTTTTTT n.269_270insTTTTTTT n.71_72insTTTTTTT | ClinVar dbSNP |
13 | g.32319080del | CA024955 | BRCA2 | c.71del (p.Leu24Ter) c.-299del (n.-299del) n.191+2553del n.269del n.71del | ClinVar dbSNP |