Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.54733154_54733155delinsATCA16602406KITc.2434_2435delinsAT (p.Asp812Ile)
n.2524_2525delinsAT
c.2431_2432delinsAT (p.Asp811Ile)
c.2449_2450delinsAT (p.Asp817Ile)
n.2858_2859delinsAT
c.2349+1156_2349+1157delinsAT (n.2349+1156_2349+1157delinsAT)
n.2604_2605delinsAT
n.243_244delinsAT
n.1458_1459delinsAT
c.2446_2447delinsAT (p.Asp816Ile)
c.1936_1937delinsAT (p.Asp646Ile)
c.2437_2438delinsAT (p.Asp813Ile)
n.2664_2665delinsAT
n.1356_1357delinsAT
c.2443_2444delinsAT (p.Asp815Ile)
n.2543_2544delinsAT
n.499_500delinsAT
ClinVar dbSNP COSMIC
4g.54733154_54733155delinsTTCA645516948KITc.2434_2435delinsTT (p.Asp812Phe)
n.2524_2525delinsTT
c.2431_2432delinsTT (p.Asp811Phe)
c.2449_2450delinsTT (p.Asp817Phe)
n.2858_2859delinsTT
c.2349+1156_2349+1157delinsTT (n.2349+1156_2349+1157delinsTT)
n.2604_2605delinsTT
n.243_244delinsTT
n.1458_1459delinsTT
c.2446_2447delinsTT (p.Asp816Phe)
c.1936_1937delinsTT (p.Asp646Phe)
c.2437_2438delinsTT (p.Asp813Phe)
n.2664_2665delinsTT
n.1356_1357delinsTT
c.2443_2444delinsTT (p.Asp815Phe)
n.2543_2544delinsTT
n.499_500delinsTT
dbSNP COSMIC

Number of alleles fetched