Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.84839718G>ACA393372474ALPK3c.439G>A (p.Ala147Thr)
c.1045G>A (p.Ala349Thr)
dbSNP gnomAD v2 gnomAD v4
15g.84839718G>CCA393372475ALPK3c.439G>C (p.Ala147Pro)
c.1045G>C (p.Ala349Pro)
15g.84839718G=CA2192416548ALPK3c.439G= (p.Ala147=)
c.1045G= (p.Ala349=)
15g.84839718G>TCA393372476ALPK3c.439G>T (p.Ala147Ser)
c.1045G>T (p.Ala349Ser)
ClinVar gnomAD v4
15g.84839719C>ACA393372479ALPK3c.440C>A (p.Ala147Asp)
c.1046C>A (p.Ala349Asp)
gnomAD v4
15g.84839719C>GCA393372478ALPK3c.440C>G (p.Ala147Gly)
c.1046C>G (p.Ala349Gly)
15g.84839719C>TCA393372477ALPK3c.440C>T (p.Ala147Val)
c.1046C>T (p.Ala349Val)
gnomAD v4
15g.84839720C>ACA492276942ALPK3c.441C>A (p.Ala147=)
c.1047C>A (p.Ala349=)
15g.84839720C>GCA492276943ALPK3c.441C>G (p.Ala147=)
c.1047C>G (p.Ala349=)
15g.84839720C>TCA492276944ALPK3c.441C>T (p.Ala147=)
c.1047C>T (p.Ala349=)
ClinVar
15g.84839721_84839722dupCA2630109255ALPK3c.442_443dup (p.Ile149ProfsTer25)
c.1048_1049dup (p.Ile351ProfsTer25)
gnomAD v4
15g.84839721G>ACA393372480ALPK3c.442G>A (p.Ala148Thr)
c.1048G>A (p.Ala350Thr)
ClinVar dbSNP gnomAD v4
15g.84839721G>CCA393372481ALPK3c.442G>C (p.Ala148Pro)
c.1048G>C (p.Ala350Pro)
15g.84839721G=CA2192416551ALPK3c.442G= (p.Ala148=)
c.1048G= (p.Ala350=)
15g.84839721G>TCA393372482ALPK3c.442G>T (p.Ala148Ser)
c.1048G>T (p.Ala350Ser)
gnomAD v4
15g.84839722C>ACA393372483ALPK3c.443C>A (p.Ala148Asp)
c.1049C>A (p.Ala350Asp)
15g.84839722C>GCA393372484ALPK3c.443C>G (p.Ala148Gly)
c.1049C>G (p.Ala350Gly)
15g.84839722C>TCA393372485ALPK3c.443C>T (p.Ala148Val)
c.1049C>T (p.Ala350Val)
COSMIC COSMIC
15g.84839723C>ACA492276951ALPK3c.444C>A (p.Ala148=)
c.1050C>A (p.Ala350=)
15g.84839723C=CA2192416555ALPK3c.444C= (p.Ala148=)
c.1050C= (p.Ala350=)
15g.84839723C>GCA7708982ALPK3c.444C>G (p.Ala148=)
c.1050C>G (p.Ala350=)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.84839723C>TCA492276952ALPK3c.444C>T (p.Ala148=)
c.1050C>T (p.Ala350=)
15g.84839724A>CCA393372486ALPK3c.445A>C (p.Ile149Leu)
c.1051A>C (p.Ile351Leu)
15g.84839724A>GCA393372488ALPK3c.445A>G (p.Ile149Val)
c.1051A>G (p.Ile351Val)
gnomAD v4
15g.84839724A>TCA393372487ALPK3c.445A>T (p.Ile149Phe)
c.1051A>T (p.Ile351Phe)
15g.84839725T>ACA393372489ALPK3c.446T>A (p.Ile149Asn)
c.1052T>A (p.Ile351Asn)
15g.84839725T>CCA7708983ALPK3c.446T>C (p.Ile149Thr)
c.1052T>C (p.Ile351Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.84839725T>GCA393372490ALPK3c.446T>G (p.Ile149Ser)
c.1052T>G (p.Ile351Ser)
15g.84839725T=CA2192416558ALPK3c.446T= (p.Ile149=)
c.1052T= (p.Ile351=)
15g.84839726C>ACA492276956ALPK3c.447C>A (p.Ile149=)
c.1053C>A (p.Ile351=)
15g.84839726C=CA2192416559ALPK3c.447C= (p.Ile149=)
c.1053C= (p.Ile351=)
15g.84839726C>GCA393372491ALPK3c.447C>G (p.Ile149Met)
c.1053C>G (p.Ile351Met)
15g.84839726C>TCA492276958ALPK3c.447C>T (p.Ile149=)
c.1053C>T (p.Ile351=)
dbSNP
15g.84839727T>ACA393372492ALPK3c.448T>A (p.Tyr150Asn)
c.1054T>A (p.Tyr352Asn)
15g.84839727T>CCA273664932ALPK3c.448T>C (p.Tyr150His)
c.1054T>C (p.Tyr352His)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC
15g.84839727T>GCA393372493ALPK3c.448T>G (p.Tyr150Asp)
c.1054T>G (p.Tyr352Asp)
15g.84839727T=CA2192416562ALPK3c.448T= (p.Tyr150=)
c.1054T= (p.Tyr352=)
15g.84839728A>CCA393372494ALPK3c.449A>C (p.Tyr150Ser)
c.1055A>C (p.Tyr352Ser)
15g.84839728A>GCA393372495ALPK3c.449A>G (p.Tyr150Cys)
c.1055A>G (p.Tyr352Cys)
15g.84839728A>TCA393372496ALPK3c.449A>T (p.Tyr150Phe)
c.1055A>T (p.Tyr352Phe)
15g.84839729C>ACA393372497ALPK3c.450C>A (p.Tyr150Ter)
c.1056C>A (p.Tyr352Ter)
15g.84839729C>GCA393372498ALPK3c.450C>G (p.Tyr150Ter)
c.1056C>G (p.Tyr352Ter)
15g.84839729C>TCA492276961ALPK3c.450C>T (p.Tyr150=)
c.1056C>T (p.Tyr352=)
15g.84839730C>ACA393372499ALPK3c.451C>A (p.Gln151Lys)
c.1057C>A (p.Gln353Lys)
15g.84839730C>GCA393372500ALPK3c.451C>G (p.Gln151Glu)
c.1057C>G (p.Gln353Glu)
15g.84839730C>TCA393372501ALPK3c.451C>T (p.Gln151Ter)
c.1057C>T (p.Gln353Ter)
15g.84839731A>CCA393372502ALPK3c.452A>C (p.Gln151Pro)
c.1058A>C (p.Gln353Pro)
15g.84839731A>GCA393372503ALPK3c.452A>G (p.Gln151Arg)
c.1058A>G (p.Gln353Arg)
15g.84839731A>TCA393372504ALPK3c.452A>T (p.Gln151Leu)
c.1058A>T (p.Gln353Leu)
15g.84839732G>ACA7708984ALPK3c.453G>A (p.Gln151=)
c.1059G>A (p.Gln353=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched