Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.108320009_108320010insCTCA168731ATM,C11orf65c.6403_6404insCT (p.Leu2135ProfsTer2)
n.2618_2619insCT
c.641-10939_641-10938insAG (p.=)
n.1807_1808insCT
c.2359_2360insCT (p.Leu787ProfsTer2)
c.6238_6239insCT (p.Leu2080ProfsTer2)
c.5359_5360insCT (p.Leu1787ProfsTer2)
c.5095_5096insCT (p.Leu1699ProfsTer2)
c.1474_1475insCT (p.Leu492ProfsTer2)
c.*39-10939_*39-10938insAG (p.=)
c.6403_6404insCT
c.2359_2360insCT
c.6238_6239insCT
c.5359_5360insCT
c.5095_5096insCT
ClinVar dbSNP
11g.108320010_108320011insTTCA350459ATM,C11orf65c.6404_6405insTT (p.Arg2136Ter)
n.2619_2620insTT
c.641-10939_641-10938insAA (p.=)
n.1808_1809insTT
c.2360_2361insTT (p.Arg788Ter)
c.6239_6240insTT (p.Arg2081Ter)
c.5360_5361insTT (p.Arg1788Ter)
c.5096_5097insTT (p.Arg1700Ter)
c.1475_1476insTT (p.Arg493Ter)
c.*39-10939_*39-10938insAA (p.=)
c.6404_6405insTT
c.2360_2361insTT
c.6239_6240insTT
c.5360_5361insTT
c.5096_5097insTT
ClinVar dbSNP dbSNP ExAC gnomAD

Number of alleles fetched