Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.39507455_39507461delCA2736037655DLL3c.1510_1516del (p.Gly504ProfsTer?)
dbSNP
19g.39507456G>ACA253978DLL3c.1511G>A (p.Gly504Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.39507456G>CCA405789119DLL3c.1511G>C (p.Gly504Ala)
19g.39507456G=CA2335548868DLL3c.1511G= (p.Gly504=)
19g.39507456G>TCA405789122DLL3c.1511G>T (p.Gly504Val)
gnomAD v4
19g.39507457C>ACA507662526DLL3c.1512C>A (p.Gly504=)
gnomAD v4
19g.39507457C>GCA507662527DLL3c.1512C>G (p.Gly504=)
19g.39507457C>TCA507662529DLL3c.1512C>T (p.Gly504=)
19g.39507458G>ACA308227752DLL3c.1513G>A (p.Val505Met)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.39507458G>CCA405789127DLL3c.1513G>C (p.Val505Leu)
19g.39507458G=CA2335548869DLL3c.1513G= (p.Val505=)
19g.39507458G>TCA405789128DLL3c.1513G>T (p.Val505Leu)
gnomAD v4
19g.39507459T>ACA405789136DLL3c.1514T>A (p.Val505Glu)
19g.39507459T>CCA405789140DLL3c.1514T>C (p.Val505Ala)
gnomAD v4
19g.39507459T>GCA405789138DLL3c.1514T>G (p.Val505Gly)
19g.39507460G>ACA507662532DLL3c.1515G>A (p.Val505=)
gnomAD v4
19g.39507460G>CCA507662534DLL3c.1515G>C (p.Val505=)
19g.39507460G>TCA507662536DLL3c.1515G>T (p.Val505=)
gnomAD v4
19g.39507461G>ACA308227757DLL3c.1516G>A (p.Ala506Thr)
dbSNP gnomAD v4
19g.39507461G>CCA405789144DLL3c.1516G>C (p.Ala506Pro)
19g.39507461G=CA2335548870DLL3c.1516G= (p.Ala506=)
19g.39507461G>TCA405789154DLL3c.1516G>T (p.Ala506Ser)
gnomAD v4
19g.39507462C>ACA405789155DLL3c.1517C>A (p.Ala506Asp)
gnomAD v4
19g.39507462C>GCA405789156DLL3c.1517C>G (p.Ala506Gly)
19g.39507462C>TCA405789157DLL3c.1517C>T (p.Ala506Val)
gnomAD v4
19g.39507463C>ACA507662539DLL3c.1518C>A (p.Ala506=)
dbSNP gnomAD v3 gnomAD v4
19g.39507463C=CA2335548871DLL3c.1518C= (p.Ala506=)
19g.39507463C>GCA507662540DLL3c.1518C>G (p.Ala506=)
gnomAD v4
19g.39507463C>TCA507662538DLL3c.1518C>T (p.Ala506=)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.39507464G>ACA405789159DLL3c.1519G>A (p.Gly507Ser)
dbSNP gnomAD v2 gnomAD v4
19g.39507464G>CCA405789161DLL3c.1519G>C (p.Gly507Arg)
dbSNP
19g.39507464G=CA2335548872DLL3c.1519G= (p.Gly507=)
19g.39507464G>TCA405789163DLL3c.1519G>T (p.Gly507Cys)
gnomAD v4
19g.39507465G>ACA405789169DLL3c.1520G>A (p.Gly507Asp)
dbSNP gnomAD v2 gnomAD v4
19g.39507465G>CCA405789172DLL3c.1520G>C (p.Gly507Ala)
gnomAD v4
19g.39507465G=CA2335548873DLL3c.1520G= (p.Gly507=)
19g.39507465G>TCA405789166DLL3c.1520G>T (p.Gly507Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.39507466C>ACA507662545DLL3c.1521C>A (p.Gly507=)
COSMIC COSMIC
19g.39507466C=CA2335548874DLL3c.1521C= (p.Gly507=)
19g.39507466C>GCA507662546DLL3c.1521C>G (p.Gly507=)
gnomAD v4
19g.39507466C>TCA9432463DLL3c.1521C>T (p.Gly507=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.39507467G>ACA405789177DLL3c.1522G>A (p.Ala508Thr)
gnomAD v4
19g.39507467G>CCA405789179DLL3c.1522G>C (p.Ala508Pro)
19g.39507467G>TCA405789181DLL3c.1522G>T (p.Ala508Ser)
gnomAD v4
19g.39507468C>ACA405789185DLL3c.1523C>A (p.Ala508Asp)
gnomAD v4
19g.39507468C>GCA405789187DLL3c.1523C>G (p.Ala508Gly)
gnomAD v4
19g.39507468C>TCA405789190DLL3c.1523C>T (p.Ala508Val)
19g.39507469T>ACA507662550DLL3c.1524T>A (p.Ala508=)
19g.39507469T>CCA507662551DLL3c.1524T>C (p.Ala508=)
gnomAD v4
19g.39507469T>GCA507662552DLL3c.1524T>G (p.Ala508=)

Number of alleles fetched