Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.40931591C>ACA489781711DLL4c.483C>A (p.Thr161=)
n.712C>A
15g.40931591C>GCA489781710DLL4c.483C>G (p.Thr161=)
n.712C>G
gnomAD v4
15g.40931591C>TCA489781709DLL4c.483C>T (p.Thr161=)
n.712C>T
gnomAD v4
15g.40931592A>CCA391806847DLL4c.484A>C (p.Ser162Arg)
n.713A>C
15g.40931592A>GCA391806848DLL4c.484A>G (p.Ser162Gly)
n.713A>G
15g.40931592A>TCA391806849DLL4c.484A>T (p.Ser162Cys)
n.713A>T
15g.40931593G>ACA391806850DLL4c.485G>A (p.Ser162Asn)
n.714G>A
dbSNP gnomAD v2 gnomAD v4
15g.40931593G>CCA391806851DLL4c.485G>C (p.Ser162Thr)
n.714G>C
15g.40931593G=CA2172012853DLL4c.485G= (p.Ser162=)
n.714G=
15g.40931593G>TCA391806852DLL4c.485G>T (p.Ser162Ile)
n.714G>T
15g.40931594C>ACA391806853DLL4c.486C>A (p.Ser162Arg)
n.715C>A
dbSNP
15g.40931594C=CA2172012854DLL4c.486C= (p.Ser162=)
n.715C=
15g.40931594C>GCA391806854DLL4c.486C>G (p.Ser162Arg)
n.715C>G
15g.40931594C>TCA489781713DLL4c.486C>T (p.Ser162=)
n.715C>T
dbSNP
15g.40931595A>CCA391806857DLL4c.487A>C (p.Thr163Pro)
n.716A>C
15g.40931595A>GCA391806855DLL4c.487A>G (p.Thr163Ala)
n.716A>G
15g.40931595A>TCA391806856DLL4c.487A>T (p.Thr163Ser)
n.716A>T
15g.40931596C>ACA391806858DLL4c.488C>A (p.Thr163Asn)
n.717C>A
15g.40931596C=CA2172012855DLL4c.488C= (p.Thr163=)
n.717C=
15g.40931596C>GCA391806859DLL4c.488C>G (p.Thr163Ser)
n.717C>G
ClinVar dbSNP
15g.40931596C>TCA391806860DLL4c.488C>T (p.Thr163Ile)
n.717C>T
dbSNP gnomAD v2 gnomAD v4
15g.40931597C>ACA7487696DLL4c.489C>A (p.Thr163=)
n.718C>A
dbSNP ExAC gnomAD v2 gnomAD v4
15g.40931597C=CA2172012856DLL4c.489C= (p.Thr163=)
n.718C=
15g.40931597C>GCA489781714DLL4c.489C>G (p.Thr163=)
n.718C>G
15g.40931597C>TCA7487695DLL4c.489C>T (p.Thr163=)
n.718C>T
dbSNP ExAC gnomAD v2 gnomAD v4
15g.40931598C>ACA391806861DLL4c.490C>A (p.Leu164Ile)
n.719C>A
15g.40931598C=CA2172012857DLL4c.490C= (p.Leu164=)
n.719C=
15g.40931598C>GCA391806862DLL4c.490C>G (p.Leu164Val)
n.719C>G
dbSNP gnomAD v4
15g.40931598C>TCA391806863DLL4c.490C>T (p.Leu164Phe)
n.719C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
15g.40931599T>ACA391806864DLL4c.491T>A (p.Leu164His)
n.720T>A
15g.40931599T>CCA391806865DLL4c.491T>C (p.Leu164Pro)
n.720T>C
15g.40931599T>GCA391806866DLL4c.491T>G (p.Leu164Arg)
n.720T>G
gnomAD v4
15g.40931600C>ACA489781715DLL4c.492C>A (p.Leu164=)
n.721C>A
15g.40931600C>GCA489781716DLL4c.492C>G (p.Leu164=)
n.721C>G
15g.40931600C>TCA489781717DLL4c.492C>T (p.Leu164=)
n.721C>T
gnomAD v4
15g.40931601A=CA2172012858DLL4c.493A= (p.Thr165=)
n.722A=
15g.40931601A>CCA391806868DLL4c.493A>C (p.Thr165Pro)
n.722A>C
15g.40931601A>GCA391806869DLL4c.493A>G (p.Thr165Ala)
n.722A>G
dbSNP gnomAD v3 gnomAD v4
15g.40931601A>TCA391806867DLL4c.493A>T (p.Thr165Ser)
n.722A>T
15g.40931602C>ACA391806870DLL4c.494C>A (p.Thr165Lys)
n.723C>A
dbSNP
15g.40931602C=CA2172012859DLL4c.494C= (p.Thr165=)
n.723C=
15g.40931602C>GCA391806871DLL4c.494C>G (p.Thr165Arg)
n.723C>G
15g.40931602C>TCA391806872DLL4c.494C>T (p.Thr165Ile)
n.723C>T
15g.40931603A>CCA489781718DLL4c.495A>C (p.Thr165=)
n.724A>C
15g.40931603A>GCA489781719DLL4c.495A>G (p.Thr165=)
n.724A>G
dbSNP
15g.40931603A>TCA489781720DLL4c.495A>T (p.Thr165=)
n.724A>T
15g.40931604A>CCA489781721DLL4c.496A>C (p.Arg166=)
n.725A>C
15g.40931604A>GCA391806873DLL4c.496A>G (p.Arg166Gly)
n.725A>G
15g.40931604A>TCA391806874DLL4c.496A>T (p.Arg166Trp)
n.725A>T
15g.40931605G>ACA391806875DLL4c.497G>A (p.Arg166Lys)
n.726G>A
dbSNP gnomAD v2

Number of alleles fetched