Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.43113628_43113629delinsTTCA007910RETc.1436_1437delinsTT (p.Cys479Phe)
n.1406_1407delinsTT
n.593_594delinsTT
c.1832_1833delinsTT (p.Cys611Phe)
c.*426_*427delinsTT (n.*426_*427delinsTT)
c.383_384delinsTT (p.Cys128Phe)
c.1289+2396_1289+2397delinsTT (n.1289+2396_1289+2397delinsTT)
c.1070_1071delinsTT (p.Cys357Phe)
dbSNP
10g.43113628_43113629delinsCTCA007903RETc.1436_1437delinsCT (p.Cys479Ser)
n.1406_1407delinsCT
n.593_594delinsCT
c.1832_1833delinsCT (p.Cys611Ser)
c.*426_*427delinsCT (n.*426_*427delinsCT)
c.383_384delinsCT (p.Cys128Ser)
c.1289+2396_1289+2397delinsCT (n.1289+2396_1289+2397delinsCT)
c.1070_1071delinsCT (p.Cys357Ser)
dbSNP
10g.43113628_43113629delinsATCA007894RETc.1436_1437delinsAT (p.Cys479Tyr)
n.1406_1407delinsAT
n.593_594delinsAT
c.1832_1833delinsAT (p.Cys611Tyr)
c.*426_*427delinsAT (n.*426_*427delinsAT)
c.383_384delinsAT (p.Cys128Tyr)
c.1289+2396_1289+2397delinsAT (n.1289+2396_1289+2397delinsAT)
c.1070_1071delinsAT (p.Cys357Tyr)
ClinVar dbSNP

Number of alleles fetched