Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.112821953C>ACA16024303APCc.1370C>A (p.Ser457Ter)
n.1426C>A
c.*1376C>A (n.*1376C>A)
c.1316C>A (p.Ser439Ter)
c.58C>A
c.5C>A (p.Ser2Ter)
c.*692C>A (n.*692C>A)
c.1400C>A (p.Ser467Ter)
c.1295C>A (p.Ser432Ter)
c.1286C>A (p.Ser429Ter)
c.1193C>A (p.Ser398Ter)
c.1097C>A (p.Ser366Ter)
c.1067C>A (p.Ser356Ter)
c.992C>A (p.Ser331Ter)
c.890C>A (p.Ser297Ter)
c.521C>A (p.Ser174Ter)
ClinVar dbSNP COSMIC
5g.112821953C>GCA16024304APCc.1370C>G (p.Ser457Ter)
n.1426C>G
c.*1376C>G (n.*1376C>G)
c.1316C>G (p.Ser439Ter)
c.58C>G
c.5C>G (p.Ser2Ter)
c.*692C>G (n.*692C>G)
c.1400C>G (p.Ser467Ter)
c.1295C>G (p.Ser432Ter)
c.1286C>G (p.Ser429Ter)
c.1193C>G (p.Ser398Ter)
c.1097C>G (p.Ser366Ter)
c.1067C>G (p.Ser356Ter)
c.992C>G (p.Ser331Ter)
c.890C>G (p.Ser297Ter)
c.521C>G (p.Ser174Ter)
ClinVar dbSNP
5g.112821953C>TCA16024305APCc.1370C>T (p.Ser457Leu)
n.1426C>T
c.*1376C>T (n.*1376C>T)
c.1316C>T (p.Ser439Leu)
c.58C>T
c.5C>T (p.Ser2Leu)
c.*692C>T (n.*692C>T)
c.1400C>T (p.Ser467Leu)
c.1295C>T (p.Ser432Leu)
c.1286C>T (p.Ser429Leu)
c.1193C>T (p.Ser398Leu)
c.1097C>T (p.Ser366Leu)
c.1067C>T (p.Ser356Leu)
c.992C>T (p.Ser331Leu)
c.890C>T (p.Ser297Leu)
c.521C>T (p.Ser174Leu)
dbSNP

Number of alleles fetched