Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55181321_55181323dupCA135857EGFR,EGFR-AS1c.2153_2155dup (p.Asn718_Pro719insHis)
c.661_663dup
c.2312_2314dup (p.Asn771_Pro772insHis)
c.*28+8393_*28+8395dup (n.*28+8393_*28+8395dup)
c.2177_2179dup (p.Asn726_Pro727insHis)
n.1248_1250dup
c.1511_1513dup (p.Asn504_Pro505insHis)
ClinVar dbSNP COSMIC
7g.55181323_55181324insACCACCCA2714508310EGFR,EGFR-AS1c.2155_2156insACCACC (p.Asn718_Pro719insHisHis)
c.663_664insACCACC
c.2314_2315insACCACC (p.Asn771_Pro772insHisHis)
c.*28+8395_*28+8396insACCACC (n.*28+8395_*28+8396insACCACC)
c.2179_2180insACCACC (p.Asn726_Pro727insHisHis)
n.1250_1251insGGTGGT
c.1513_1514insACCACC (p.Asn504_Pro505insHisHis)
dbSNP
7g.55181323_55181324insGGCACCCA645561598EGFR,EGFR-AS1c.2155_2156insGGCACC (p.Asn718_Pro719insArgHis)
c.663_664insGGCACC
c.2314_2315insGGCACC (p.Asn771_Pro772insArgHis)
c.*28+8395_*28+8396insGGCACC (n.*28+8395_*28+8396insGGCACC)
c.2179_2180insGGCACC (p.Asn726_Pro727insArgHis)
n.1250_1251insGCCGGT
c.1513_1514insGGCACC (p.Asn504_Pro505insArgHis)
dbSNP COSMIC

Number of alleles fetched