Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.95096519_95096520delCA16619898DICER1c.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
14g.95096517_95096520delCA916081732DICER1c.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

Number of alleles fetched