Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.21568023_21568029delinsAGTCCAGCA1158016102ALPLc.649-81_649-75delinsAGTCCAG (n.649-81_649-75delinsAGTCCAG)
c.418-81_418-75delinsAGTCCAG (n.418-81_418-75delinsAGTCCAG)
c.484-81_484-75delinsAGTCCAG (n.484-81_484-75delinsAGTCCAG)
c.493-81_493-75delinsAGTCCAG (n.493-81_493-75delinsAGTCCAG)
1g.21568026_21568031delCA731318719ALPLc.649-78_649-73del (n.649-78_649-73del)
c.418-78_418-73del (n.418-78_418-73del)
c.484-78_484-73del (n.484-78_484-73del)
c.493-78_493-73del (n.493-78_493-73del)
 dbSNP
1g.21568028A>CCA2574253105ALPLc.649-76A>C (n.649-76A>C)
c.418-76A>C (n.418-76A>C)
c.484-76A>C (n.484-76A>C)
c.493-76A>C (n.493-76A>C)
1g.21568028A>GCA2643930750ALPLc.649-76A>G (n.649-76A>G)
c.418-76A>G (n.418-76A>G)
c.484-76A>G (n.484-76A>G)
c.493-76A>G (n.493-76A>G)
 gnomAD v4
1g.21568029G>ACA1158016103ALPLc.649-75G>A (n.649-75G>A)
c.418-75G>A (n.418-75G>A)
c.484-75G>A (n.484-75G>A)
c.493-75G>A (n.493-75G>A)
 dbSNP gnomAD v4
1g.21568029G>CCA913224399ALPLc.649-75G>C (n.649-75G>C)
c.418-75G>C (n.418-75G>C)
c.484-75G>C (n.484-75G>C)
c.493-75G>C (n.493-75G>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.21568029G=CA1158016104ALPLc.649-75G= (n.649-75G=)
c.418-75G= (n.418-75G=)
c.484-75G= (n.484-75G=)
c.493-75G= (n.493-75G=)
1g.21568030G>ACA2643930753ALPLc.649-74G>A (n.649-74G>A)
c.418-74G>A (n.418-74G>A)
c.484-74G>A (n.484-74G>A)
c.493-74G>A (n.493-74G>A)
 gnomAD v4
1g.21568030G>CCA2643930754ALPLc.649-74G>C (n.649-74G>C)
c.418-74G>C (n.418-74G>C)
c.484-74G>C (n.484-74G>C)
c.493-74G>C (n.493-74G>C)
 gnomAD v4
1g.21568031T>CCA2643930755ALPLc.649-73T>C (n.649-73T>C)
c.418-73T>C (n.418-73T>C)
c.484-73T>C (n.484-73T>C)
c.493-73T>C (n.493-73T>C)
 gnomAD v4
1g.21568032T>GCA731318724ALPLc.649-72T>G (n.649-72T>G)
c.418-72T>G (n.418-72T>G)
c.484-72T>G (n.484-72T>G)
c.493-72T>G (n.493-72T>G)
 dbSNP
1g.21568032T=CA1158016105ALPLc.649-72T= (n.649-72T=)
c.418-72T= (n.418-72T=)
c.484-72T= (n.484-72T=)
c.493-72T= (n.493-72T=)
1g.21568033C=CA1158016106ALPLc.649-71C= (n.649-71C=)
c.418-71C= (n.418-71C=)
c.484-71C= (n.484-71C=)
c.493-71C= (n.493-71C=)
1g.21568033C>TCA999407008ALPLc.649-71C>T (n.649-71C>T)
c.418-71C>T (n.418-71C>T)
c.484-71C>T (n.484-71C>T)
c.493-71C>T (n.493-71C>T)
 dbSNP gnomAD v3 gnomAD v4
1g.21568034C>ACA2643930756ALPLc.649-70C>A (n.649-70C>A)
c.418-70C>A (n.418-70C>A)
c.484-70C>A (n.484-70C>A)
c.493-70C>A (n.493-70C>A)
 gnomAD v4
1g.21568035A>GCA2643930757ALPLc.649-69A>G (n.649-69A>G)
c.418-69A>G (n.418-69A>G)
c.484-69A>G (n.484-69A>G)
c.493-69A>G (n.493-69A>G)
 gnomAD v4
1g.21568036delCA2643930758ALPLc.649-68del (n.649-68del)
c.418-68del (n.418-68del)
c.484-68del (n.484-68del)
c.493-68del (n.493-68del)
 gnomAD v4
1g.21568039C>ACA2574253107ALPLc.649-65C>A (n.649-65C>A)
c.418-65C>A (n.418-65C>A)
c.484-65C>A (n.484-65C>A)
c.493-65C>A (n.493-65C>A)
1g.21568039C=CA1158016107ALPLc.649-65C= (n.649-65C=)
c.418-65C= (n.418-65C=)
c.484-65C= (n.484-65C=)
c.493-65C= (n.493-65C=)
1g.21568039C>TCA19063241ALPLc.649-65C>T (n.649-65C>T)
c.418-65C>T (n.418-65C>T)
c.484-65C>T (n.484-65C>T)
c.493-65C>T (n.493-65C>T)
 dbSNP gnomAD v3 gnomAD v4
1g.21568040G>ACA19063252ALPLc.649-64G>A (n.649-64G>A)
c.418-64G>A (n.418-64G>A)
c.484-64G>A (n.484-64G>A)
c.493-64G>A (n.493-64G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.21568040G=CA1158016108ALPLc.649-64G= (n.649-64G=)
c.418-64G= (n.418-64G=)
c.484-64G= (n.484-64G=)
c.493-64G= (n.493-64G=)
1g.21568041A>GCA2742753731ALPLc.649-63A>G (n.649-63A>G)
c.418-63A>G (n.418-63A>G)
c.484-63A>G (n.484-63A>G)
c.493-63A>G (n.493-63A>G)
1g.21568043G>ACA2643930760ALPLc.649-61G>A (n.649-61G>A)
c.418-61G>A (n.418-61G>A)
c.484-61G>A (n.484-61G>A)
c.493-61G>A (n.493-61G>A)
 gnomAD v4
1g.21568043G>CCA999407018ALPLc.649-61G>C (n.649-61G>C)
c.418-61G>C (n.418-61G>C)
c.484-61G>C (n.484-61G>C)
c.493-61G>C (n.493-61G>C)
 dbSNP gnomAD v3 gnomAD v4
1g.21568043G=CA1158016109ALPLc.649-61G= (n.649-61G=)
c.418-61G= (n.418-61G=)
c.484-61G= (n.484-61G=)
c.493-61G= (n.493-61G=)
1g.21568045C>ACA2643930762ALPLc.649-59C>A (n.649-59C>A)
c.418-59C>A (n.418-59C>A)
c.484-59C>A (n.484-59C>A)
c.493-59C>A (n.493-59C>A)
 gnomAD v4
1g.21568046A=CA1158016110ALPLc.649-58A= (n.649-58A=)
c.418-58A= (n.418-58A=)
c.484-58A= (n.484-58A=)
c.493-58A= (n.493-58A=)
1g.21568046A>CCA1158016111ALPLc.649-58A>C (n.649-58A>C)
c.418-58A>C (n.418-58A>C)
c.484-58A>C (n.484-58A>C)
c.493-58A>C (n.493-58A>C)
 dbSNP gnomAD v4
1g.21568046A>TCA2643930763ALPLc.649-58A>T (n.649-58A>T)
c.418-58A>T (n.418-58A>T)
c.484-58A>T (n.484-58A>T)
c.493-58A>T (n.493-58A>T)
 gnomAD v4
1g.21568047C>ACA2742753733ALPLc.649-57C>A (n.649-57C>A)
c.418-57C>A (n.418-57C>A)
c.484-57C>A (n.484-57C>A)
c.493-57C>A (n.493-57C>A)
1g.21568047C=CA1140829556ALPLc.649-57C= (n.649-57C=)
c.418-57C= (n.418-57C=)
c.484-57C= (n.484-57C=)
c.493-57C= (n.493-57C=)
1g.21568047C>GCA19063256ALPLc.649-57C>G (n.649-57C>G)
c.418-57C>G (n.418-57C>G)
c.484-57C>G (n.484-57C>G)
c.493-57C>G (n.493-57C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.21568049G>ACA2643930765ALPLc.649-55G>A (n.649-55G>A)
c.418-55G>A (n.418-55G>A)
c.484-55G>A (n.484-55G>A)
c.493-55G>A (n.493-55G>A)
 gnomAD v4
1g.21568049G>TCA2574253110ALPLc.649-55G>T (n.649-55G>T)
c.418-55G>T (n.418-55G>T)
c.484-55G>T (n.484-55G>T)
c.493-55G>T (n.493-55G>T)
1g.21568050G>TCA2643930766ALPLc.649-54G>T (n.649-54G>T)
c.418-54G>T (n.418-54G>T)
c.484-54G>T (n.484-54G>T)
c.493-54G>T (n.493-54G>T)
 gnomAD v4
1g.21568051G>ACA2574253111ALPLc.649-53G>A (n.649-53G>A)
c.418-53G>A (n.418-53G>A)
c.484-53G>A (n.484-53G>A)
c.493-53G>A (n.493-53G>A)
 gnomAD v4
1g.21568052G>ACA521577200ALPLc.649-52G>A (n.649-52G>A)
c.418-52G>A (n.418-52G>A)
c.484-52G>A (n.484-52G>A)
c.493-52G>A (n.493-52G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.21568052G=CA1158016112ALPLc.649-52G= (n.649-52G=)
c.418-52G= (n.418-52G=)
c.484-52G= (n.484-52G=)
c.493-52G= (n.493-52G=)
1g.21568054T>CCA666558ALPLc.649-50T>C (n.649-50T>C)
c.418-50T>C (n.418-50T>C)
c.484-50T>C (n.484-50T>C)
c.493-50T>C (n.493-50T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568054T=CA1158016113ALPLc.649-50T= (n.649-50T=)
c.418-50T= (n.418-50T=)
c.484-50T= (n.484-50T=)
c.493-50T= (n.493-50T=)
1g.21568056C>TCA2695500424ALPLc.649-48C>T (n.649-48C>T)
c.418-48C>T (n.418-48C>T)
c.484-48C>T (n.484-48C>T)
c.493-48C>T (n.493-48C>T)
 dbSNP
1g.21568059G>TCA645684321ALPLc.649-45G>T (n.649-45G>T)
c.418-45G>T (n.418-45G>T)
c.484-45G>T (n.484-45G>T)
c.493-45G>T (n.493-45G>T)
 gnomAD v4 COSMIC
1g.21568060G>ACA1158016114ALPLc.649-44G>A (n.649-44G>A)
c.418-44G>A (n.418-44G>A)
c.484-44G>A (n.484-44G>A)
c.493-44G>A (n.493-44G>A)
 dbSNP
1g.21568060G=CA1158016115ALPLc.649-44G= (n.649-44G=)
c.418-44G= (n.418-44G=)
c.484-44G= (n.484-44G=)
c.493-44G= (n.493-44G=)
1g.21568060G>TCA666559ALPLc.649-44G>T (n.649-44G>T)
c.418-44G>T (n.418-44G>T)
c.484-44G>T (n.484-44G>T)
c.493-44G>T (n.493-44G>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568061C>TCA2643930767ALPLc.649-43C>T (n.649-43C>T)
c.418-43C>T (n.418-43C>T)
c.484-43C>T (n.484-43C>T)
c.493-43C>T (n.493-43C>T)
 gnomAD v4
1g.21568062A=CA1158016116ALPLc.649-42A= (n.649-42A=)
c.418-42A= (n.418-42A=)
c.484-42A= (n.484-42A=)
c.493-42A= (n.493-42A=)
1g.21568062A>GCA666560ALPLc.649-42A>G (n.649-42A>G)
c.418-42A>G (n.418-42A>G)
c.484-42A>G (n.484-42A>G)
c.493-42A>G (n.493-42A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.21568063dupCA2574253113ALPLc.649-41dup (n.649-41dup)
c.418-41dup (n.418-41dup)
c.484-41dup (n.484-41dup)
c.493-41dup (n.493-41dup)
1g.21568064C=CA1158016117ALPLc.649-40C= (n.649-40C=)
c.418-40C= (n.418-40C=)
c.484-40C= (n.484-40C=)
c.493-40C= (n.493-40C=)
1g.21568064C>GCA19063269ALPLc.649-40C>G (n.649-40C>G)
c.418-40C>G (n.418-40C>G)
c.484-40C>G (n.484-40C>G)
c.493-40C>G (n.493-40C>G)
 dbSNP gnomAD v4
1g.21568066delCA2643930768ALPLc.649-38del (n.649-38del)
c.418-38del (n.418-38del)
c.484-38del (n.484-38del)
c.493-38del (n.493-38del)
 gnomAD v4
1g.21568067G>ACA2742753735ALPLc.649-37G>A (n.649-37G>A)
c.418-37G>A (n.418-37G>A)
c.484-37G>A (n.484-37G>A)
c.493-37G>A (n.493-37G>A)
1g.21568069A=CA1158016118ALPLc.649-35A= (n.649-35A=)
c.418-35A= (n.418-35A=)
c.484-35A= (n.484-35A=)
c.493-35A= (n.493-35A=)
1g.21568069A>TCA666561ALPLc.649-35A>T (n.649-35A>T)
c.418-35A>T (n.418-35A>T)
c.484-35A>T (n.484-35A>T)
c.493-35A>T (n.493-35A>T)
 dbSNP ExAC gnomAD v2
1g.21568071C>TCA2643930769ALPLc.649-33C>T (n.649-33C>T)
c.418-33C>T (n.418-33C>T)
c.484-33C>T (n.484-33C>T)
c.493-33C>T (n.493-33C>T)
 gnomAD v4
1g.21568073C>GCA2643930770ALPLc.649-31C>G (n.649-31C>G)
c.418-31C>G (n.418-31C>G)
c.484-31C>G (n.484-31C>G)
c.493-31C>G (n.493-31C>G)
 gnomAD v4
1g.21568075_21568076delinsGCCA1158016119ALPLc.649-29_649-28delinsGC (n.649-29_649-28delinsGC)
c.418-29_418-28delinsGC (n.418-29_418-28delinsGC)
c.484-29_484-28delinsGC (n.484-29_484-28delinsGC)
c.493-29_493-28delinsGC (n.493-29_493-28delinsGC)
1g.21568076delCA666562ALPLc.649-28del (n.649-28del)
c.418-28del (n.418-28del)
c.484-28del (n.484-28del)
c.493-28del (n.493-28del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568076C=CA1158016120ALPLc.649-28C= (n.649-28C=)
c.418-28C= (n.418-28C=)
c.484-28C= (n.484-28C=)
c.493-28C= (n.493-28C=)
1g.21568076C>TCA999407029ALPLc.649-28C>T (n.649-28C>T)
c.418-28C>T (n.418-28C>T)
c.484-28C>T (n.484-28C>T)
c.493-28C>T (n.493-28C>T)
 dbSNP gnomAD v3 gnomAD v4
1g.21568077A=CA1158016121ALPLc.649-27A= (n.649-27A=)
c.418-27A= (n.418-27A=)
c.484-27A= (n.484-27A=)
c.493-27A= (n.493-27A=)
1g.21568077A>GCA521577201ALPLc.649-27A>G (n.649-27A>G)
c.418-27A>G (n.418-27A>G)
c.484-27A>G (n.484-27A>G)
c.493-27A>G (n.493-27A>G)
 dbSNP gnomAD v2 gnomAD v4
1g.21568079A>GCA2574253115ALPLc.649-25A>G (n.649-25A>G)
c.418-25A>G (n.418-25A>G)
c.484-25A>G (n.484-25A>G)
c.493-25A>G (n.493-25A>G)
 gnomAD v4
1g.21568081G>ACA666563ALPLc.649-23G>A (n.649-23G>A)
c.418-23G>A (n.418-23G>A)
c.484-23G>A (n.484-23G>A)
c.493-23G>A (n.493-23G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568081G=CA1158016122ALPLc.649-23G= (n.649-23G=)
c.418-23G= (n.418-23G=)
c.484-23G= (n.484-23G=)
c.493-23G= (n.493-23G=)
1g.21568083G>TCA2594139765ALPLc.649-21G>T (n.649-21G>T)
c.418-21G>T (n.418-21G>T)
c.484-21G>T (n.484-21G>T)
c.493-21G>T (n.493-21G>T)
 gnomAD v3 gnomAD v4
1g.21568084A=CA1158016123ALPLc.649-20A= (n.649-20A=)
c.418-20A= (n.418-20A=)
c.484-20A= (n.484-20A=)
c.493-20A= (n.493-20A=)
1g.21568084A>TCA1158016124ALPLc.649-20A>T (n.649-20A>T)
c.418-20A>T (n.418-20A>T)
c.484-20A>T (n.484-20A>T)
c.493-20A>T (n.493-20A>T)
 dbSNP
1g.21568088C>TCA2695500508ALPLc.649-16C>T (n.649-16C>T)
c.418-16C>T (n.418-16C>T)
c.484-16C>T (n.484-16C>T)
c.493-16C>T (n.493-16C>T)
 dbSNP
1g.21568089T>ACA2643930773ALPLc.649-15T>A (n.649-15T>A)
c.418-15T>A (n.418-15T>A)
c.484-15T>A (n.484-15T>A)
c.493-15T>A (n.493-15T>A)
 gnomAD v4
1g.21568089T>GCA666564ALPLc.649-15T>G (n.649-15T>G)
c.418-15T>G (n.418-15T>G)
c.484-15T>G (n.484-15T>G)
c.493-15T>G (n.493-15T>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568089T=CA1143851980ALPLc.649-15T= (n.649-15T=)
c.418-15T= (n.418-15T=)
c.484-15T= (n.484-15T=)
c.493-15T= (n.493-15T=)
1g.21568090C>GCA645684322ALPLc.649-14C>G (n.649-14C>G)
c.418-14C>G (n.418-14C>G)
c.484-14C>G (n.484-14C>G)
c.493-14C>G (n.493-14C>G)
 COSMIC
1g.21568090C>TCA2643930774ALPLc.649-14C>T (n.649-14C>T)
c.418-14C>T (n.418-14C>T)
c.484-14C>T (n.484-14C>T)
c.493-14C>T (n.493-14C>T)
 ClinVar gnomAD v4
1g.21568092delCA2742753737ALPLc.649-12del (n.649-12del)
c.418-12del (n.418-12del)
c.484-12del (n.484-12del)
c.493-12del (n.493-12del)
1g.21568093G>ACA731318750ALPLc.649-11G>A (n.649-11G>A)
c.418-11G>A (n.418-11G>A)
c.484-11G>A (n.484-11G>A)
c.493-11G>A (n.493-11G>A)
 dbSNP gnomAD v4
1g.21568093G>CCA666565ALPLc.649-11G>C (n.649-11G>C)
c.418-11G>C (n.418-11G>C)
c.484-11G>C (n.484-11G>C)
c.493-11G>C (n.493-11G>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568093G=CA1144134554ALPLc.649-11G= (n.649-11G=)
c.418-11G= (n.418-11G=)
c.484-11G= (n.484-11G=)
c.493-11G= (n.493-11G=)
1g.21568094T>ACA2574253119ALPLc.649-10T>A (n.649-10T>A)
c.418-10T>A (n.418-10T>A)
c.484-10T>A (n.484-10T>A)
c.493-10T>A (n.493-10T>A)
 ClinVar
1g.21568096delCA2499214452ALPLc.649-8del (n.649-8del)
c.418-8del (n.418-8del)
c.484-8del (n.484-8del)
c.493-8del (n.493-8del)
 ClinVar dbSNP
1g.21568096T>CCA2580061473ALPLc.649-8T>C (n.649-8T>C)
c.418-8T>C (n.418-8T>C)
c.484-8T>C (n.484-8T>C)
c.493-8T>C (n.493-8T>C)
 ClinVar
1g.21568098T>CCA2643930775ALPLc.649-6T>C (n.649-6T>C)
c.418-6T>C (n.418-6T>C)
c.484-6T>C (n.484-6T>C)
c.493-6T>C (n.493-6T>C)
 gnomAD v4
1g.21568100_21568101delCA2739272371ALPLc.649-4_649-3del (n.649-4_649-3del)
c.418-4_418-3del (n.418-4_418-3del)
c.484-4_484-3del (n.484-4_484-3del)
c.493-4_493-3del (n.493-4_493-3del)
 ClinVar
1g.21568100T>GCA2574253120ALPLc.649-4T>G (n.649-4T>G)
c.418-4T>G (n.418-4T>G)
c.484-4T>G (n.484-4T>G)
c.493-4T>G (n.493-4T>G)
 ClinVar gnomAD v4
1g.21568101T>CCA2580061474ALPLc.649-3T>C (n.649-3T>C)
c.418-3T>C (n.418-3T>C)
c.484-3T>C (n.484-3T>C)
c.493-3T>C (n.493-3T>C)
 ClinVar
1g.21568101_21568103delinsAACA2586964039ALPLc.649-3_649-1delinsAA (n.649-3_649-1delinsAA)
c.418-3_418-1delinsAA (n.418-3_418-1delinsAA)
c.484-3_484-1delinsAA (n.484-3_484-1delinsAA)
c.493-3_493-1delinsAA (n.493-3_493-1delinsAA)
1g.21568102A>CCA338878997ALPLc.649-2A>C (n.649-2A>C)
c.418-2A>C (n.418-2A>C)
c.484-2A>C (n.484-2A>C)
c.493-2A>C (n.493-2A>C)
1g.21568102A>GCA338878995ALPLc.649-2A>G (n.649-2A>G)
c.418-2A>G (n.418-2A>G)
c.484-2A>G (n.484-2A>G)
c.493-2A>G (n.493-2A>G)
1g.21568102A>TCA338878993ALPLc.649-2A>T (n.649-2A>T)
c.418-2A>T (n.418-2A>T)
c.484-2A>T (n.484-2A>T)
c.493-2A>T (n.493-2A>T)
1g.21568103G>ACA338878999ALPLc.649-1G>A (n.649-1G>A)
c.418-1G>A (n.418-1G>A)
c.484-1G>A (n.484-1G>A)
c.493-1G>A (n.493-1G>A)
 ClinVar dbSNP
1g.21568103G>CCA338879000ALPLc.649-1G>C (n.649-1G>C)
c.418-1G>C (n.418-1G>C)
c.484-1G>C (n.484-1G>C)
c.493-1G>C (n.493-1G>C)
 gnomAD v4
1g.21568103G>TCA338879002ALPLc.649-1G>T (n.649-1G>T)
c.418-1G>T (n.418-1G>T)
c.484-1G>T (n.484-1G>T)
c.493-1G>T (n.493-1G>T)
1g.21568104G>ACA338879003ALPLc.649G>A (p.Val217Met)
c.418G>A (p.Val140Met)
c.484G>A (p.Val162Met)
c.493G>A (p.Val165Met)
 dbSNP
1g.21568104G>CCA338879005ALPLc.649G>C (p.Val217Leu)
c.418G>C (p.Val140Leu)
c.484G>C (p.Val162Leu)
c.493G>C (p.Val165Leu)
1g.21568104G=CA1158016125ALPLc.649G= (p.Val217=)
c.418G= (p.Val140=)
c.484G= (p.Val162=)
c.493G= (p.Val165=)
1g.21568104G>TCA338879007ALPLc.649G>T (p.Val217Leu)
c.418G>T (p.Val140Leu)
c.484G>T (p.Val162Leu)
c.493G>T (p.Val165Leu)
1g.21568104_21568105delinsGTCA1158016126ALPLc.649_650delinsGT (p.Val217=)
c.418_419delinsGT (p.Val140=)
c.484_485delinsGT (p.Val162=)
c.493_494delinsGT (p.Val165=)
1g.21568104_21568105insCCA666566ALPLc.649_650insC (p.Val217AlafsTer15)
c.418_419insC (p.Val140AlafsTer15)
c.484_485insC (p.Val162AlafsTer15)
c.493_494insC (p.Val165AlafsTer15)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568104_21568105insCTACA1158016128ALPLc.649_650insCTA (p.Val217delinsAlaMet)
c.418_419insCTA (p.Val140delinsAlaMet)
c.484_485insCTA (p.Val162delinsAlaMet)
c.493_494insCTA (p.Val165delinsAlaMet)
 ClinVar dbSNP
1g.21568105T>ACA338879010ALPLc.650T>A (p.Val217Glu)
c.419T>A (p.Val140Glu)
c.485T>A (p.Val162Glu)
c.494T>A (p.Val165Glu)
 dbSNP
1g.21568105T>CCA666567ALPLc.650T>C (p.Val217Ala)
c.419T>C (p.Val140Ala)
c.485T>C (p.Val162Ala)
c.494T>C (p.Val165Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568105T>GCA338879011ALPLc.650T>G (p.Val217Gly)
c.419T>G (p.Val140Gly)
c.485T>G (p.Val162Gly)
c.494T>G (p.Val165Gly)
1g.21568105T=CA1158016127ALPLc.650T= (p.Val217=)
c.419T= (p.Val140=)
c.485T= (p.Val162=)
c.494T= (p.Val165=)
1g.21568105delinsCTAACA658820988ALPLc.650delinsCTAA (p.Val217delinsAlaLys)
c.419delinsCTAA (p.Val140delinsAlaLys)
c.485delinsCTAA (p.Val162delinsAlaLys)
c.494delinsCTAA (p.Val165delinsAlaLys)
 ClinVar dbSNP
1g.21568105_21568106insAACA666568ALPLc.650_651insAA (p.Ile218ArgfsTer?)
c.419_420insAA (p.Ile141ArgfsTer?)
c.485_486insAA (p.Ile163ArgfsTer?)
c.494_495insAA (p.Ile166ArgfsTer?)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568106G>ACA416529862ALPLc.651G>A (p.Val217=)
c.420G>A (p.Val140=)
c.486G>A (p.Val162=)
c.495G>A (p.Val165=)
1g.21568106G>CCA416529864ALPLc.651G>C (p.Val217=)
c.420G>C (p.Val140=)
c.486G>C (p.Val162=)
c.495G>C (p.Val165=)
1g.21568106G>TCA416529867ALPLc.651G>T (p.Val217=)
c.420G>T (p.Val140=)
c.486G>T (p.Val162=)
c.495G>T (p.Val165=)
1g.21568107A>CCA338879014ALPLc.652A>C (p.Ile218Leu)
c.421A>C (p.Ile141Leu)
c.487A>C (p.Ile163Leu)
c.496A>C (p.Ile166Leu)
1g.21568107A>GCA338879015ALPLc.652A>G (p.Ile218Val)
c.421A>G (p.Ile141Val)
c.487A>G (p.Ile163Val)
c.496A>G (p.Ile166Val)
1g.21568107A>TCA338879016ALPLc.652A>T (p.Ile218Phe)
c.421A>T (p.Ile141Phe)
c.487A>T (p.Ile163Phe)
c.496A>T (p.Ile166Phe)
1g.21568108T>ACA666569ALPLc.653T>A (p.Ile218Asn)
c.422T>A (p.Ile141Asn)
c.488T>A (p.Ile163Asn)
c.497T>A (p.Ile166Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.21568108T>CCA338879021ALPLc.653T>C (p.Ile218Thr)
c.422T>C (p.Ile141Thr)
c.488T>C (p.Ile163Thr)
c.497T>C (p.Ile166Thr)
 gnomAD v4
1g.21568108T>GCA338879019ALPLc.653T>G (p.Ile218Ser)
c.422T>G (p.Ile141Ser)
c.488T>G (p.Ile163Ser)
c.497T>G (p.Ile166Ser)
1g.21568108T=CA1148278875ALPLc.653T= (p.Ile218=)
c.422T= (p.Ile141=)
c.488T= (p.Ile163=)
c.497T= (p.Ile166=)
1g.21568109C>ACA416529879ALPLc.654C>A (p.Ile218=)
c.423C>A (p.Ile141=)
c.489C>A (p.Ile163=)
c.498C>A (p.Ile166=)
1g.21568109C>GCA338879022ALPLc.654C>G (p.Ile218Met)
c.423C>G (p.Ile141Met)
c.489C>G (p.Ile163Met)
c.498C>G (p.Ile166Met)
 gnomAD v4
1g.21568109C>TCA416529877ALPLc.654C>T (p.Ile218=)
c.423C>T (p.Ile141=)
c.489C>T (p.Ile163=)
c.498C>T (p.Ile166=)
 COSMIC
1g.21568110A=CA1158016129ALPLc.655A= (p.Met219=)
c.424A= (p.Met142=)
c.490A= (p.Met164=)
c.499A= (p.Met167=)
1g.21568110A>CCA338879024ALPLc.655A>C (p.Met219Leu)
c.424A>C (p.Met142Leu)
c.490A>C (p.Met164Leu)
c.499A>C (p.Met167Leu)
 dbSNP
1g.21568110A>GCA666570ALPLc.655A>G (p.Met219Val)
c.424A>G (p.Met142Val)
c.490A>G (p.Met164Val)
c.499A>G (p.Met167Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568110A>TCA338879027ALPLc.655A>T (p.Met219Leu)
c.424A>T (p.Met142Leu)
c.490A>T (p.Met164Leu)
c.499A>T (p.Met167Leu)
1g.21568111T>ACA338879029ALPLc.656T>A (p.Met219Lys)
c.425T>A (p.Met142Lys)
c.491T>A (p.Met164Lys)
c.500T>A (p.Met167Lys)
1g.21568111T>CCA338879031ALPLc.656T>C (p.Met219Thr)
c.425T>C (p.Met142Thr)
c.491T>C (p.Met164Thr)
c.500T>C (p.Met167Thr)
 dbSNP gnomAD v2 gnomAD v4
1g.21568111T>GCA338879032ALPLc.656T>G (p.Met219Arg)
c.425T>G (p.Met142Arg)
c.491T>G (p.Met164Arg)
c.500T>G (p.Met167Arg)
1g.21568111T=CA1158016131ALPLc.656T= (p.Met219=)
c.425T= (p.Met142=)
c.491T= (p.Met164=)
c.500T= (p.Met167=)
1g.21568111_21568112delinsTGCA1158016130ALPLc.656_657delinsTG (p.Met219=)
c.425_426delinsTG (p.Met142=)
c.491_492delinsTG (p.Met164=)
c.500_501delinsTG (p.Met167=)
1g.21568112G>ACA338879036ALPLc.657G>A (p.Met219Ile)
c.426G>A (p.Met142Ile)
c.492G>A (p.Met164Ile)
c.501G>A (p.Met167Ile)
1g.21568112G>CCA338879037ALPLc.657G>C (p.Met219Ile)
c.426G>C (p.Met142Ile)
c.492G>C (p.Met164Ile)
c.501G>C (p.Met167Ile)
1g.21568112G=CA1158016132ALPLc.657G= (p.Met219=)
c.426G= (p.Met142=)
c.492G= (p.Met164=)
c.501G= (p.Met167=)
1g.21568112G>TCA666572ALPLc.657G>T (p.Met219Ile)
c.426G>T (p.Met142Ile)
c.492G>T (p.Met164Ile)
c.501G>T (p.Met167Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.21568117dupCA16040717ALPLc.662dup (p.Gly222TrpfsTer10)
c.431dup (p.Gly145TrpfsTer10)
c.497dup (p.Gly167TrpfsTer10)
c.506dup (p.Gly170TrpfsTer10)
 ClinVar dbSNP gnomAD v4
1g.21568117delCA666571ALPLc.662del (p.Gly221ValfsTer?)
c.431del (p.Gly144ValfsTer?)
c.497del (p.Gly166ValfsTer?)
c.506del (p.Gly169ValfsTer?)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.21568113G>ACA666573ALPLc.658G>A (p.Gly220Arg)
c.427G>A (p.Gly143Arg)
c.493G>A (p.Gly165Arg)
c.502G>A (p.Gly168Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.21568113G>CCA338879042ALPLc.658G>C (p.Gly220Arg)
c.427G>C (p.Gly143Arg)
c.493G>C (p.Gly165Arg)
c.502G>C (p.Gly168Arg)
1g.21568113G=CA1148465515ALPLc.658G= (p.Gly220=)
c.427G= (p.Gly143=)
c.493G= (p.Gly165=)
c.502G= (p.Gly168=)
1g.21568113G>TCA338879044ALPLc.658G>T (p.Gly220Trp)
c.427G>T (p.Gly143Trp)
c.493G>T (p.Gly165Trp)
c.502G>T (p.Gly168Trp)
1g.21568114G>ACA338879047ALPLc.659G>A (p.Gly220Glu)
c.428G>A (p.Gly143Glu)
c.494G>A (p.Gly165Glu)
c.503G>A (p.Gly168Glu)
 ClinVar gnomAD v4
1g.21568114G>CCA338879046ALPLc.659G>C (p.Gly220Ala)
c.428G>C (p.Gly143Ala)
c.494G>C (p.Gly165Ala)
c.503G>C (p.Gly168Ala)
 ClinVar dbSNP gnomAD v4
1g.21568114G=CA1158016133ALPLc.659G= (p.Gly220=)
c.428G= (p.Gly143=)
c.494G= (p.Gly165=)
c.503G= (p.Gly168=)
1g.21568114G>TCA338879049ALPLc.659G>T (p.Gly220Val)
c.428G>T (p.Gly143Val)
c.494G>T (p.Gly165Val)
c.503G>T (p.Gly168Val)
 ClinVar dbSNP gnomAD v4
1g.21568115G>ACA416529895ALPLc.660G>A (p.Gly220=)
c.429G>A (p.Gly143=)
c.495G>A (p.Gly165=)
c.504G>A (p.Gly168=)
1g.21568115G>CCA416529896ALPLc.660G>C (p.Gly220=)
c.429G>C (p.Gly143=)
c.495G>C (p.Gly165=)
c.504G>C (p.Gly168=)
1g.21568115G=CA1158016134ALPLc.660G= (p.Gly220=)
c.429G= (p.Gly143=)
c.495G= (p.Gly165=)
c.504G= (p.Gly168=)
1g.21568115G>TCA416529893ALPLc.660G>T (p.Gly220=)
c.429G>T (p.Gly143=)
c.495G>T (p.Gly165=)
c.504G>T (p.Gly168=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.21568116G>ACA338879051ALPLc.661G>A (p.Gly221Ser)
c.430G>A (p.Gly144Ser)
c.496G>A (p.Gly166Ser)
c.505G>A (p.Gly169Ser)
1g.21568116G>CCA666574ALPLc.661G>C (p.Gly221Arg)
c.430G>C (p.Gly144Arg)
c.496G>C (p.Gly166Arg)
c.505G>C (p.Gly169Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.21568116G=CA1158016135ALPLc.661G= (p.Gly221=)
c.430G= (p.Gly144=)
c.496G= (p.Gly166=)
c.505G= (p.Gly169=)
1g.21568116G>TCA338879053ALPLc.661G>T (p.Gly221Cys)
c.430G>T (p.Gly144Cys)
c.496G>T (p.Gly166Cys)
c.505G>T (p.Gly169Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.21568117G>ACA338879056ALPLc.662G>A (p.Gly221Asp)
c.431G>A (p.Gly144Asp)
c.497G>A (p.Gly166Asp)
c.506G>A (p.Gly169Asp)
1g.21568117G>CCA666575ALPLc.662G>C (p.Gly221Ala)
c.431G>C (p.Gly144Ala)
c.497G>C (p.Gly166Ala)
c.506G>C (p.Gly169Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568117G=CA1147211666ALPLc.662G= (p.Gly221=)
c.431G= (p.Gly144=)
c.497G= (p.Gly166=)
c.506G= (p.Gly169=)
1g.21568117G>TCA666576ALPLc.662G>T (p.Gly221Val)
c.431G>T (p.Gly144Val)
c.497G>T (p.Gly166Val)
c.506G>T (p.Gly169Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568118T>ACA416529904ALPLc.663T>A (p.Gly221=)
c.432T>A (p.Gly144=)
c.498T>A (p.Gly166=)
c.507T>A (p.Gly169=)
1g.21568118T>CCA416529903ALPLc.663T>C (p.Gly221=)
c.432T>C (p.Gly144=)
c.498T>C (p.Gly166=)
c.507T>C (p.Gly169=)
 gnomAD v4
1g.21568118T>GCA416529905ALPLc.663T>G (p.Gly221=)
c.432T>G (p.Gly144=)
c.498T>G (p.Gly166=)
c.507T>G (p.Gly169=)
 dbSNP
1g.21568118T=CA1158016136ALPLc.663T= (p.Gly221=)
c.432T= (p.Gly144=)
c.498T= (p.Gly166=)
c.507T= (p.Gly169=)
1g.21568119G>ACA338879058ALPLc.664G>A (p.Gly222Ser)
c.433G>A (p.Gly145Ser)
c.499G>A (p.Gly167Ser)
c.508G>A (p.Gly170Ser)
1g.21568119G>CCA338879060ALPLc.664G>C (p.Gly222Arg)
c.433G>C (p.Gly145Arg)
c.499G>C (p.Gly167Arg)
c.508G>C (p.Gly170Arg)
1g.21568119G>TCA338879062ALPLc.664G>T (p.Gly222Cys)
c.433G>T (p.Gly145Cys)
c.499G>T (p.Gly167Cys)
c.508G>T (p.Gly170Cys)
1g.21568120G>ACA338879064ALPLc.665G>A (p.Gly222Asp)
c.434G>A (p.Gly145Asp)
c.500G>A (p.Gly167Asp)
c.509G>A (p.Gly170Asp)
1g.21568120G>CCA338879065ALPLc.665G>C (p.Gly222Ala)
c.434G>C (p.Gly145Ala)
c.500G>C (p.Gly167Ala)
c.509G>C (p.Gly170Ala)
1g.21568120G>TCA338879067ALPLc.665G>T (p.Gly222Val)
c.434G>T (p.Gly145Val)
c.500G>T (p.Gly167Val)
c.509G>T (p.Gly170Val)
1g.21568121C>ACA416529913ALPLc.666C>A (p.Gly222=)
c.435C>A (p.Gly145=)
c.501C>A (p.Gly167=)
c.510C>A (p.Gly170=)
1g.21568121C>GCA416529915ALPLc.666C>G (p.Gly222=)
c.435C>G (p.Gly145=)
c.501C>G (p.Gly167=)
c.510C>G (p.Gly170=)
1g.21568121C>TCA416529912ALPLc.666C>T (p.Gly222=)
c.435C>T (p.Gly145=)
c.501C>T (p.Gly167=)
c.510C>T (p.Gly170=)
 ClinVar
1g.21568122C>ACA416529917ALPLc.667C>A (p.Arg223=)
c.436C>A (p.Arg146=)
c.502C>A (p.Arg168=)
c.511C>A (p.Arg171=)
1g.21568122C=CA1158016137ALPLc.667C= (p.Arg223=)
c.436C= (p.Arg146=)
c.502C= (p.Arg168=)
c.511C= (p.Arg171=)
1g.21568122C>GCA338879068ALPLc.667C>G (p.Arg223Gly)
c.436C>G (p.Arg146Gly)
c.502C>G (p.Arg168Gly)
c.511C>G (p.Arg171Gly)
1g.21568122C>TCA274235ALPLc.667C>T (p.Arg223Trp)
c.436C>T (p.Arg146Trp)
c.502C>T (p.Arg168Trp)
c.511C>T (p.Arg171Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.21568123G>ACA666577ALPLc.668G>A (p.Arg223Gln)
c.437G>A (p.Arg146Gln)
c.503G>A (p.Arg168Gln)
c.512G>A (p.Arg171Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568123G>CCA338879072ALPLc.668G>C (p.Arg223Pro)
c.437G>C (p.Arg146Pro)
c.503G>C (p.Arg168Pro)
c.512G>C (p.Arg171Pro)
1g.21568123G=CA1143366460ALPLc.668G= (p.Arg223=)
c.437G= (p.Arg146=)
c.503G= (p.Arg168=)
c.512G= (p.Arg171=)
1g.21568123G>TCA338879074ALPLc.668G>T (p.Arg223Leu)
c.437G>T (p.Arg146Leu)
c.503G>T (p.Arg168Leu)
c.512G>T (p.Arg171Leu)
 gnomAD v4
1g.21568124G>ACA416529926ALPLc.669G>A (p.Arg223=)
c.438G>A (p.Arg146=)
c.504G>A (p.Arg168=)
c.513G>A (p.Arg171=)
 ClinVar
1g.21568124G>CCA416529922ALPLc.669G>C (p.Arg223=)
c.438G>C (p.Arg146=)
c.504G>C (p.Arg168=)
c.513G>C (p.Arg171=)
1g.21568124G>TCA416529924ALPLc.669G>T (p.Arg223=)
c.438G>T (p.Arg146=)
c.504G>T (p.Arg168=)
c.513G>T (p.Arg171=)
 gnomAD v4
1g.21568125A=CA1158016138ALPLc.670A= (p.Lys224=)
c.439A= (p.Lys147=)
c.505A= (p.Lys169=)
c.514A= (p.Lys172=)
1g.21568125A>CCA338879079ALPLc.670A>C (p.Lys224Gln)
c.439A>C (p.Lys147Gln)
c.505A>C (p.Lys169Gln)
c.514A>C (p.Lys172Gln)
1g.21568125A>GCA338879076ALPLc.670A>G (p.Lys224Glu)
c.439A>G (p.Lys147Glu)
c.505A>G (p.Lys169Glu)
c.514A>G (p.Lys172Glu)
 ClinVar dbSNP gnomAD v4
1g.21568125A>TCA338879078ALPLc.670A>T (p.Lys224Ter)
c.439A>T (p.Lys147Ter)
c.505A>T (p.Lys169Ter)
c.514A>T (p.Lys172Ter)
1g.21568126A>CCA338879081ALPLc.671A>C (p.Lys224Thr)
c.440A>C (p.Lys147Thr)
c.506A>C (p.Lys169Thr)
c.515A>C (p.Lys172Thr)
1g.21568126A>GCA338879082ALPLc.671A>G (p.Lys224Arg)
c.440A>G (p.Lys147Arg)
c.506A>G (p.Lys169Arg)
c.515A>G (p.Lys172Arg)
1g.21568126A>TCA338879084ALPLc.671A>T (p.Lys224Ile)
c.440A>T (p.Lys147Ile)
c.506A>T (p.Lys169Ile)
c.515A>T (p.Lys172Ile)
 ClinVar
1g.21568127A>CCA338879086ALPLc.672A>C (p.Lys224Asn)
c.441A>C (p.Lys147Asn)
c.507A>C (p.Lys169Asn)
c.516A>C (p.Lys172Asn)
1g.21568127A>GCA416529932ALPLc.672A>G (p.Lys224=)
c.441A>G (p.Lys147=)
c.507A>G (p.Lys169=)
c.516A>G (p.Lys172=)
1g.21568127A>TCA338879087ALPLc.672A>T (p.Lys224Asn)
c.441A>T (p.Lys147Asn)
c.507A>T (p.Lys169Asn)
c.516A>T (p.Lys172Asn)
1g.21568128T>ACA338879089ALPLc.673T>A (p.Tyr225Asn)
c.442T>A (p.Tyr148Asn)
c.508T>A (p.Tyr170Asn)
c.517T>A (p.Tyr173Asn)
1g.21568128T>CCA666578ALPLc.673T>C (p.Tyr225His)
c.442T>C (p.Tyr148His)
c.508T>C (p.Tyr170His)
c.517T>C (p.Tyr173His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.21568128T>GCA338879091ALPLc.673T>G (p.Tyr225Asp)
c.442T>G (p.Tyr148Asp)
c.508T>G (p.Tyr170Asp)
c.517T>G (p.Tyr173Asp)
1g.21568128T=CA1158016139ALPLc.673T= (p.Tyr225=)
c.442T= (p.Tyr148=)
c.508T= (p.Tyr170=)
c.517T= (p.Tyr173=)

Number of alleles fetched