Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.95096519_95096520del | CA16619898 | DICER1 | c.4405_4406del (p.Leu1469PhefsTer7) c.*1055_*1056del (n.*1055_*1056del) n.1392_1393del n.4668_4669del n.5511_5512del n.4814_4815del c.2150_2151del (n.2150_2151del) c.*2721_*2722del (n.*2721_*2722del) c.440_441del c.1099_1100del (p.Leu367PhefsTer7) c.4000_4001del (p.Leu1334PhefsTer7) c.2926_2927del (p.Leu976PhefsTer7) c.4123_4124del (p.Leu1375PhefsTer7) c.3838_3839del (p.Leu1280PhefsTer7) c.2722_2723del (p.Leu908PhefsTer7) n.4823_4824del n.5007_5008del n.4917_4918del n.4840_4841del n.4673_4674del n.4750_4751del | ClinVar dbSNP |
14 | g.95096517_95096520del | CA916081732 | DICER1 | c.4403_4406del (p.Ser1468PhefsTer21) c.*1053_*1056del (n.*1053_*1056del) n.1390_1393del n.4666_4669del n.5509_5512del n.4812_4815del c.2148_2151del (n.2148_2151del) c.*2719_*2722del (n.*2719_*2722del) c.438_441del c.1097_1100del (p.Ser366PhefsTer21) c.3998_4001del (p.Ser1333PhefsTer21) c.2924_2927del (p.Ser975PhefsTer21) c.4121_4124del (p.Ser1374PhefsTer21) c.3836_3839del (p.Ser1279PhefsTer21) c.2720_2723del (p.Ser907PhefsTer21) n.4821_4824del n.5005_5008del n.4915_4918del n.4838_4841del n.4671_4674del n.4748_4751del | ClinVar dbSNP |