Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108687510_108687545dupCA259023COL4A5c.4344_4379dup (p.Gly1460_Thr1461insProAspGlyLeuGlnGlyProProGlyProProGly)
c.4326_4361dup (p.Gly1454_Thr1455insProAspGlyLeuGlnGlyProProGlyProProGly)
n.838_873dup
c.140_175dup
c.4335_4370dup (p.Gly1457_Thr1458insProAspGlyLeuGlnGlyProProGlyProProGly)
c.4020_4055dup (p.Gly1352_Thr1353insProAspGlyLeuGlnGlyProProGlyProProGly)
c.1917_1952dup (p.Gly651_Thr652insProAspGlyLeuGlnGlyProProGlyProProGly)
c.4359_4394dup (p.Gly1465_Thr1466insProAspGlyLeuGlnGlyProProGlyProProGly)
c.4350_4385dup (p.Gly1462_Thr1463insProAspGlyLeuGlnGlyProProGlyProProGly)
c.4341_4376dup (p.Gly1459_Thr1460insProAspGlyLeuGlnGlyProProGlyProProGly)
c.2679_2714dup (p.Gly905_Thr906insProAspGlyLeuGlnGlyProProGlyProProGly)
dbSNP
Xg.108687513_108687539delCA259030COL4A5c.4347_4373del (p.Asp1450_Pro1458del)
c.4329_4355del (p.Asp1444_Pro1452del)
n.841_867del
c.143_169del
c.4338_4364del (p.Asp1447_Pro1455del)
c.4023_4049del (p.Asp1342_Pro1350del)
c.1920_1946del (p.Asp641_Pro649del)
c.4362_4388del (p.Asp1455_Pro1463del)
c.4353_4379del (p.Asp1452_Pro1460del)
c.4344_4370del (p.Asp1449_Pro1457del)
c.2682_2708del (p.Asp895_Pro903del)
dbSNP
Xg.108687535G>ACA259033COL4A5c.4369G>A (p.Gly1457Ser)
c.4351G>A (p.Gly1451Ser)
n.863G>A
c.165G>A
c.4360G>A (p.Gly1454Ser)
c.4045G>A (p.Gly1349Ser)
c.1942G>A (p.Gly648Ser)
c.4384G>A (p.Gly1462Ser)
c.4375G>A (p.Gly1459Ser)
c.4366G>A (p.Gly1456Ser)
c.2704G>A (p.Gly902Ser)
dbSNP
Xg.108687535G>CCA413854092COL4A5c.4369G>C (p.Gly1457Arg)
c.4351G>C (p.Gly1451Arg)
n.863G>C
c.165G>C
c.4360G>C (p.Gly1454Arg)
c.4045G>C (p.Gly1349Arg)
c.1942G>C (p.Gly648Arg)
c.4384G>C (p.Gly1462Arg)
c.4375G>C (p.Gly1459Arg)
c.4366G>C (p.Gly1456Arg)
c.2704G>C (p.Gly902Arg)
Xg.108687535G=CA2450719245COL4A5c.4369G= (p.Gly1457=)
c.4351G= (p.Gly1451=)
n.863G=
c.165G=
c.4360G= (p.Gly1454=)
c.4045G= (p.Gly1349=)
c.1942G= (p.Gly648=)
c.4384G= (p.Gly1462=)
c.4375G= (p.Gly1459=)
c.4366G= (p.Gly1456=)
c.2704G= (p.Gly902=)
Xg.108687535G>TCA413854094COL4A5c.4369G>T (p.Gly1457Cys)
c.4351G>T (p.Gly1451Cys)
n.863G>T
c.165G>T
c.4360G>T (p.Gly1454Cys)
c.4045G>T (p.Gly1349Cys)
c.1942G>T (p.Gly648Cys)
c.4384G>T (p.Gly1462Cys)
c.4375G>T (p.Gly1459Cys)
c.4366G>T (p.Gly1456Cys)
c.2704G>T (p.Gly902Cys)
Xg.108687536G>ACA413854096COL4A5c.4370G>A (p.Gly1457Asp)
c.4352G>A (p.Gly1451Asp)
n.864G>A
c.166G>A
c.4361G>A (p.Gly1454Asp)
c.4046G>A (p.Gly1349Asp)
c.1943G>A (p.Gly648Asp)
c.4385G>A (p.Gly1462Asp)
c.4376G>A (p.Gly1459Asp)
c.4367G>A (p.Gly1456Asp)
c.2705G>A (p.Gly902Asp)
gnomAD v4
Xg.108687536G>CCA413854097COL4A5c.4370G>C (p.Gly1457Ala)
c.4352G>C (p.Gly1451Ala)
n.864G>C
c.166G>C
c.4361G>C (p.Gly1454Ala)
c.4046G>C (p.Gly1349Ala)
c.1943G>C (p.Gly648Ala)
c.4385G>C (p.Gly1462Ala)
c.4376G>C (p.Gly1459Ala)
c.4367G>C (p.Gly1456Ala)
c.2705G>C (p.Gly902Ala)
Xg.108687536G=CA2450719248COL4A5c.4370G= (p.Gly1457=)
c.4352G= (p.Gly1451=)
n.864G=
c.166G=
c.4361G= (p.Gly1454=)
c.4046G= (p.Gly1349=)
c.1943G= (p.Gly648=)
c.4385G= (p.Gly1462=)
c.4376G= (p.Gly1459=)
c.4367G= (p.Gly1456=)
c.2705G= (p.Gly902=)
Xg.108687536G>TCA413854099COL4A5c.4370G>T (p.Gly1457Val)
c.4352G>T (p.Gly1451Val)
n.864G>T
c.166G>T
c.4361G>T (p.Gly1454Val)
c.4046G>T (p.Gly1349Val)
c.1943G>T (p.Gly648Val)
c.4385G>T (p.Gly1462Val)
c.4376G>T (p.Gly1459Val)
c.4367G>T (p.Gly1456Val)
c.2705G>T (p.Gly902Val)
Xg.108687537T>ACA517924495COL4A5c.4371T>A (p.Gly1457=)
c.4353T>A (p.Gly1451=)
n.865T>A
c.167T>A
c.4362T>A (p.Gly1454=)
c.4047T>A (p.Gly1349=)
c.1944T>A (p.Gly648=)
c.4386T>A (p.Gly1462=)
c.4377T>A (p.Gly1459=)
c.4368T>A (p.Gly1456=)
c.2706T>A (p.Gly902=)
Xg.108687537T>CCA517924496COL4A5c.4371T>C (p.Gly1457=)
c.4353T>C (p.Gly1451=)
n.865T>C
c.167T>C
c.4362T>C (p.Gly1454=)
c.4047T>C (p.Gly1349=)
c.1944T>C (p.Gly648=)
c.4386T>C (p.Gly1462=)
c.4377T>C (p.Gly1459=)
c.4368T>C (p.Gly1456=)
c.2706T>C (p.Gly902=)
gnomAD v4
Xg.108687537T>GCA517924497COL4A5c.4371T>G (p.Gly1457=)
c.4353T>G (p.Gly1451=)
n.865T>G
c.167T>G
c.4362T>G (p.Gly1454=)
c.4047T>G (p.Gly1349=)
c.1944T>G (p.Gly648=)
c.4386T>G (p.Gly1462=)
c.4377T>G (p.Gly1459=)
c.4368T>G (p.Gly1456=)
c.2706T>G (p.Gly902=)
ClinVar gnomAD v4
Xg.108687537T=CA2450719249COL4A5c.4371T= (p.Gly1457=)
c.4353T= (p.Gly1451=)
n.865T=
c.167T=
c.4362T= (p.Gly1454=)
c.4047T= (p.Gly1349=)
c.1944T= (p.Gly648=)
c.4386T= (p.Gly1462=)
c.4377T= (p.Gly1459=)
c.4368T= (p.Gly1456=)
c.2706T= (p.Gly902=)
Xg.108687538C>ACA413854101COL4A5c.4372C>A (p.Pro1458Thr)
c.4354C>A (p.Pro1452Thr)
n.866C>A
c.168C>A
c.4363C>A (p.Pro1455Thr)
c.4048C>A (p.Pro1350Thr)
c.1945C>A (p.Pro649Thr)
c.4387C>A (p.Pro1463Thr)
c.4378C>A (p.Pro1460Thr)
c.4369C>A (p.Pro1457Thr)
c.2707C>A (p.Pro903Thr)
Xg.108687538C=CA2450719252COL4A5c.4372C= (p.Pro1458=)
c.4354C= (p.Pro1452=)
n.866C=
c.168C=
c.4363C= (p.Pro1455=)
c.4048C= (p.Pro1350=)
c.1945C= (p.Pro649=)
c.4387C= (p.Pro1463=)
c.4378C= (p.Pro1460=)
c.4369C= (p.Pro1457=)
c.2707C= (p.Pro903=)
Xg.108687538C>GCA413854103COL4A5c.4372C>G (p.Pro1458Ala)
c.4354C>G (p.Pro1452Ala)
n.866C>G
c.168C>G
c.4363C>G (p.Pro1455Ala)
c.4048C>G (p.Pro1350Ala)
c.1945C>G (p.Pro649Ala)
c.4387C>G (p.Pro1463Ala)
c.4378C>G (p.Pro1460Ala)
c.4369C>G (p.Pro1457Ala)
c.2707C>G (p.Pro903Ala)
Xg.108687538C>TCA413854102COL4A5c.4372C>T (p.Pro1458Ser)
c.4354C>T (p.Pro1452Ser)
n.866C>T
c.168C>T
c.4363C>T (p.Pro1455Ser)
c.4048C>T (p.Pro1350Ser)
c.1945C>T (p.Pro649Ser)
c.4387C>T (p.Pro1463Ser)
c.4378C>T (p.Pro1460Ser)
c.4369C>T (p.Pro1457Ser)
c.2707C>T (p.Pro903Ser)
ClinVar dbSNP gnomAD v4
Xg.108687542dupCA2450719251COL4A5c.4376dup (p.Gly1460TrpfsTer?)
c.4358dup (p.Gly1454TrpfsTer?)
n.870dup
c.172dup
c.4367dup (p.Gly1457TrpfsTer?)
c.4052dup (p.Gly1352TrpfsTer?)
c.1949dup (p.Gly651TrpfsTer?)
c.4391dup (p.Gly1465TrpfsTer?)
c.4382dup (p.Gly1462TrpfsTer?)
c.4373dup (p.Gly1459TrpfsTer?)
c.2711dup (p.Gly905TrpfsTer?)
ClinVar dbSNP
Xg.108687542delCA2579677161COL4A5c.4376del (p.Pro1459LeufsTer?)
c.4358del (p.Pro1453LeufsTer?)
n.870del
c.172del
c.4367del (p.Pro1456LeufsTer?)
c.4052del (p.Pro1351LeufsTer?)
c.1949del (p.Pro650LeufsTer?)
c.4391del (p.Pro1464LeufsTer?)
c.4382del (p.Pro1461LeufsTer?)
c.4373del (p.Pro1458LeufsTer?)
c.2711del (p.Pro904LeufsTer?)
Xg.108687539C>ACA413854104COL4A5c.4373C>A (p.Pro1458His)
c.4355C>A (p.Pro1452His)
n.867C>A
c.169C>A
c.4364C>A (p.Pro1455His)
c.4049C>A (p.Pro1350His)
c.1946C>A (p.Pro649His)
c.4388C>A (p.Pro1463His)
c.4379C>A (p.Pro1460His)
c.4370C>A (p.Pro1457His)
c.2708C>A (p.Pro903His)
Xg.108687539C>GCA413854105COL4A5c.4373C>G (p.Pro1458Arg)
c.4355C>G (p.Pro1452Arg)
n.867C>G
c.169C>G
c.4364C>G (p.Pro1455Arg)
c.4049C>G (p.Pro1350Arg)
c.1946C>G (p.Pro649Arg)
c.4388C>G (p.Pro1463Arg)
c.4379C>G (p.Pro1460Arg)
c.4370C>G (p.Pro1457Arg)
c.2708C>G (p.Pro903Arg)
Xg.108687539C>TCA413854106COL4A5c.4373C>T (p.Pro1458Leu)
c.4355C>T (p.Pro1452Leu)
n.867C>T
c.169C>T
c.4364C>T (p.Pro1455Leu)
c.4049C>T (p.Pro1350Leu)
c.1946C>T (p.Pro649Leu)
c.4388C>T (p.Pro1463Leu)
c.4379C>T (p.Pro1460Leu)
c.4370C>T (p.Pro1457Leu)
c.2708C>T (p.Pro903Leu)
gnomAD v4
Xg.108687540C>ACA517924504COL4A5c.4374C>A (p.Pro1458=)
c.4356C>A (p.Pro1452=)
n.868C>A
c.170C>A
c.4365C>A (p.Pro1455=)
c.4050C>A (p.Pro1350=)
c.1947C>A (p.Pro649=)
c.4389C>A (p.Pro1463=)
c.4380C>A (p.Pro1460=)
c.4371C>A (p.Pro1457=)
c.2709C>A (p.Pro903=)
Xg.108687540C>GCA517924508COL4A5c.4374C>G (p.Pro1458=)
c.4356C>G (p.Pro1452=)
n.868C>G
c.170C>G
c.4365C>G (p.Pro1455=)
c.4050C>G (p.Pro1350=)
c.1947C>G (p.Pro649=)
c.4389C>G (p.Pro1463=)
c.4380C>G (p.Pro1460=)
c.4371C>G (p.Pro1457=)
c.2709C>G (p.Pro903=)
Xg.108687540C>TCA517924505COL4A5c.4374C>T (p.Pro1458=)
c.4356C>T (p.Pro1452=)
n.868C>T
c.170C>T
c.4365C>T (p.Pro1455=)
c.4050C>T (p.Pro1350=)
c.1947C>T (p.Pro649=)
c.4389C>T (p.Pro1463=)
c.4380C>T (p.Pro1460=)
c.4371C>T (p.Pro1457=)
c.2709C>T (p.Pro903=)
ClinVar dbSNP
Xg.108687541C>ACA413854107COL4A5c.4375C>A (p.Pro1459Thr)
c.4357C>A (p.Pro1453Thr)
n.869C>A
c.171C>A
c.4366C>A (p.Pro1456Thr)
c.4051C>A (p.Pro1351Thr)
c.1948C>A (p.Pro650Thr)
c.4390C>A (p.Pro1464Thr)
c.4381C>A (p.Pro1461Thr)
c.4372C>A (p.Pro1458Thr)
c.2710C>A (p.Pro904Thr)
COSMIC COSMIC
Xg.108687541C>GCA413854108COL4A5c.4375C>G (p.Pro1459Ala)
c.4357C>G (p.Pro1453Ala)
n.869C>G
c.171C>G
c.4366C>G (p.Pro1456Ala)
c.4051C>G (p.Pro1351Ala)
c.1948C>G (p.Pro650Ala)
c.4390C>G (p.Pro1464Ala)
c.4381C>G (p.Pro1461Ala)
c.4372C>G (p.Pro1458Ala)
c.2710C>G (p.Pro904Ala)
Xg.108687541C>TCA413854109COL4A5c.4375C>T (p.Pro1459Ser)
c.4357C>T (p.Pro1453Ser)
n.869C>T
c.171C>T
c.4366C>T (p.Pro1456Ser)
c.4051C>T (p.Pro1351Ser)
c.1948C>T (p.Pro650Ser)
c.4390C>T (p.Pro1464Ser)
c.4381C>T (p.Pro1461Ser)
c.4372C>T (p.Pro1458Ser)
c.2710C>T (p.Pro904Ser)
Xg.108687542C>ACA413854111COL4A5c.4376C>A (p.Pro1459His)
c.4358C>A (p.Pro1453His)
n.870C>A
c.172C>A
c.4367C>A (p.Pro1456His)
c.4052C>A (p.Pro1351His)
c.1949C>A (p.Pro650His)
c.4391C>A (p.Pro1464His)
c.4382C>A (p.Pro1461His)
c.4373C>A (p.Pro1458His)
c.2711C>A (p.Pro904His)
Xg.108687542C>GCA413854112COL4A5c.4376C>G (p.Pro1459Arg)
c.4358C>G (p.Pro1453Arg)
n.870C>G
c.172C>G
c.4367C>G (p.Pro1456Arg)
c.4052C>G (p.Pro1351Arg)
c.1949C>G (p.Pro650Arg)
c.4391C>G (p.Pro1464Arg)
c.4382C>G (p.Pro1461Arg)
c.4373C>G (p.Pro1458Arg)
c.2711C>G (p.Pro904Arg)
Xg.108687542C>TCA413854115COL4A5c.4376C>T (p.Pro1459Leu)
c.4358C>T (p.Pro1453Leu)
n.870C>T
c.172C>T
c.4367C>T (p.Pro1456Leu)
c.4052C>T (p.Pro1351Leu)
c.1949C>T (p.Pro650Leu)
c.4391C>T (p.Pro1464Leu)
c.4382C>T (p.Pro1461Leu)
c.4373C>T (p.Pro1458Leu)
c.2711C>T (p.Pro904Leu)
Xg.108687542_108687543delinsCTCA2450719253COL4A5c.4376_4377delinsCT (p.Pro1459=)
c.4358_4359delinsCT (p.Pro1453=)
n.870_871delinsCT
c.172_173delinsCT
c.4367_4368delinsCT (p.Pro1456=)
c.4052_4053delinsCT (p.Pro1351=)
c.1949_1950delinsCT (p.Pro650=)
c.4391_4392delinsCT (p.Pro1464=)
c.4382_4383delinsCT (p.Pro1461=)
c.4373_4374delinsCT (p.Pro1458=)
c.2711_2712delinsCT (p.Pro904=)
Xg.108687543delCA915951311COL4A5c.4377del (p.Gly1460GlufsTer?)
c.4359del (p.Gly1454GlufsTer?)
n.871del
c.173del
c.4368del (p.Gly1457GlufsTer?)
c.4053del (p.Gly1352GlufsTer?)
c.1950del (p.Gly651GlufsTer?)
c.4392del (p.Gly1465GlufsTer?)
c.4383del (p.Gly1462GlufsTer?)
c.4374del (p.Gly1459GlufsTer?)
c.2712del (p.Gly905GlufsTer?)
ClinVar dbSNP
Xg.108687543T>ACA517924513COL4A5c.4377T>A (p.Pro1459=)
c.4359T>A (p.Pro1453=)
n.871T>A
c.173T>A
c.4368T>A (p.Pro1456=)
c.4053T>A (p.Pro1351=)
c.1950T>A (p.Pro650=)
c.4392T>A (p.Pro1464=)
c.4383T>A (p.Pro1461=)
c.4374T>A (p.Pro1458=)
c.2712T>A (p.Pro904=)
COSMIC COSMIC
Xg.108687543T>CCA517924515COL4A5c.4377T>C (p.Pro1459=)
c.4359T>C (p.Pro1453=)
n.871T>C
c.173T>C
c.4368T>C (p.Pro1456=)
c.4053T>C (p.Pro1351=)
c.1950T>C (p.Pro650=)
c.4392T>C (p.Pro1464=)
c.4383T>C (p.Pro1461=)
c.4374T>C (p.Pro1458=)
c.2712T>C (p.Pro904=)
Xg.108687543T>GCA517924516COL4A5c.4377T>G (p.Pro1459=)
c.4359T>G (p.Pro1453=)
n.871T>G
c.173T>G
c.4368T>G (p.Pro1456=)
c.4053T>G (p.Pro1351=)
c.1950T>G (p.Pro650=)
c.4392T>G (p.Pro1464=)
c.4383T>G (p.Pro1461=)
c.4374T>G (p.Pro1458=)
c.2712T>G (p.Pro904=)
Xg.108687544G>ACA413854117COL4A5c.4378G>A (p.Gly1460Arg)
c.4360G>A (p.Gly1454Arg)
n.872G>A
c.174G>A
c.4369G>A (p.Gly1457Arg)
c.4054G>A (p.Gly1352Arg)
c.1951G>A (p.Gly651Arg)
c.4393G>A (p.Gly1465Arg)
c.4384G>A (p.Gly1462Arg)
c.4375G>A (p.Gly1459Arg)
c.2713G>A (p.Gly905Arg)
Xg.108687544G>CCA413854118COL4A5c.4378G>C (p.Gly1460Arg)
c.4360G>C (p.Gly1454Arg)
n.872G>C
c.174G>C
c.4369G>C (p.Gly1457Arg)
c.4054G>C (p.Gly1352Arg)
c.1951G>C (p.Gly651Arg)
c.4393G>C (p.Gly1465Arg)
c.4384G>C (p.Gly1462Arg)
c.4375G>C (p.Gly1459Arg)
c.2713G>C (p.Gly905Arg)
Xg.108687544G>TCA413854119COL4A5c.4378G>T (p.Gly1460Ter)
c.4360G>T (p.Gly1454Ter)
n.872G>T
c.174G>T
c.4369G>T (p.Gly1457Ter)
c.4054G>T (p.Gly1352Ter)
c.1951G>T (p.Gly651Ter)
c.4393G>T (p.Gly1465Ter)
c.4384G>T (p.Gly1462Ter)
c.4375G>T (p.Gly1459Ter)
c.2713G>T (p.Gly905Ter)
Xg.108687544_108687545insACA2580100168COL4A5c.4378_4379insA (p.Gly1460GlufsTer?)
c.4360_4361insA (p.Gly1454GlufsTer?)
n.872_873insA
c.174_175insA
c.4369_4370insA (p.Gly1457GlufsTer?)
c.4054_4055insA (p.Gly1352GlufsTer?)
c.1951_1952insA (p.Gly651GlufsTer?)
c.4393_4394insA (p.Gly1465GlufsTer?)
c.4384_4385insA (p.Gly1462GlufsTer?)
c.4375_4376insA (p.Gly1459GlufsTer?)
c.2713_2714insA (p.Gly905GlufsTer?)
ClinVar
Xg.108687545G>ACA413854120COL4A5c.4379G>A (p.Gly1460Glu)
c.4361G>A (p.Gly1454Glu)
n.873G>A
c.175G>A
c.4370G>A (p.Gly1457Glu)
c.4055G>A (p.Gly1352Glu)
c.1952G>A (p.Gly651Glu)
c.4394G>A (p.Gly1465Glu)
c.4385G>A (p.Gly1462Glu)
c.4376G>A (p.Gly1459Glu)
c.2714G>A (p.Gly905Glu)
gnomAD v4
Xg.108687545G>CCA413854122COL4A5c.4379G>C (p.Gly1460Ala)
c.4361G>C (p.Gly1454Ala)
n.873G>C
c.175G>C
c.4370G>C (p.Gly1457Ala)
c.4055G>C (p.Gly1352Ala)
c.1952G>C (p.Gly651Ala)
c.4394G>C (p.Gly1465Ala)
c.4385G>C (p.Gly1462Ala)
c.4376G>C (p.Gly1459Ala)
c.2714G>C (p.Gly905Ala)
Xg.108687545G>TCA413854121COL4A5c.4379G>T (p.Gly1460Val)
c.4361G>T (p.Gly1454Val)
n.873G>T
c.175G>T
c.4370G>T (p.Gly1457Val)
c.4055G>T (p.Gly1352Val)
c.1952G>T (p.Gly651Val)
c.4394G>T (p.Gly1465Val)
c.4385G>T (p.Gly1462Val)
c.4376G>T (p.Gly1459Val)
c.2714G>T (p.Gly905Val)
Xg.108687546A>CCA517924521COL4A5c.4380A>C (p.Gly1460=)
c.4362A>C (p.Gly1454=)
n.874A>C
c.176A>C
c.4371A>C (p.Gly1457=)
c.4056A>C (p.Gly1352=)
c.1953A>C (p.Gly651=)
c.4395A>C (p.Gly1465=)
c.4386A>C (p.Gly1462=)
c.4377A>C (p.Gly1459=)
c.2715A>C (p.Gly905=)
gnomAD v4
Xg.108687546A>GCA517924522COL4A5c.4380A>G (p.Gly1460=)
c.4362A>G (p.Gly1454=)
n.874A>G
c.176A>G
c.4371A>G (p.Gly1457=)
c.4056A>G (p.Gly1352=)
c.1953A>G (p.Gly651=)
c.4395A>G (p.Gly1465=)
c.4386A>G (p.Gly1462=)
c.4377A>G (p.Gly1459=)
c.2715A>G (p.Gly905=)
Xg.108687546A>TCA517924523COL4A5c.4380A>T (p.Gly1460=)
c.4362A>T (p.Gly1454=)
n.874A>T
c.176A>T
c.4371A>T (p.Gly1457=)
c.4056A>T (p.Gly1352=)
c.1953A>T (p.Gly651=)
c.4395A>T (p.Gly1465=)
c.4386A>T (p.Gly1462=)
c.4377A>T (p.Gly1459=)
c.2715A>T (p.Gly905=)
Xg.108687547A>CCA413854124COL4A5c.4381A>C (p.Thr1461Pro)
c.4363A>C (p.Thr1455Pro)
n.875A>C
c.177A>C
c.4372A>C (p.Thr1458Pro)
c.4057A>C (p.Thr1353Pro)
c.1954A>C (p.Thr652Pro)
c.4396A>C (p.Thr1466Pro)
c.4387A>C (p.Thr1463Pro)
c.4378A>C (p.Thr1460Pro)
c.2716A>C (p.Thr906Pro)
Xg.108687547A>GCA413854129COL4A5c.4381A>G (p.Thr1461Ala)
c.4363A>G (p.Thr1455Ala)
n.875A>G
c.177A>G
c.4372A>G (p.Thr1458Ala)
c.4057A>G (p.Thr1353Ala)
c.1954A>G (p.Thr652Ala)
c.4396A>G (p.Thr1466Ala)
c.4387A>G (p.Thr1463Ala)
c.4378A>G (p.Thr1460Ala)
c.2716A>G (p.Thr906Ala)
Xg.108687547A>TCA413854131COL4A5c.4381A>T (p.Thr1461Ser)
c.4363A>T (p.Thr1455Ser)
n.875A>T
c.177A>T
c.4372A>T (p.Thr1458Ser)
c.4057A>T (p.Thr1353Ser)
c.1954A>T (p.Thr652Ser)
c.4396A>T (p.Thr1466Ser)
c.4387A>T (p.Thr1463Ser)
c.4378A>T (p.Thr1460Ser)
c.2716A>T (p.Thr906Ser)

Number of alleles fetched