Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108687488_108687515delinsGTGGTTTGGATGGTCCCCCTGGTCCAGACA2450719203COL4A5c.4322_4349delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA (p.Arg1441=)
c.4304_4331delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA (p.Arg1435=)
n.816_843delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA
c.118_145delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA
c.4313_4340delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA (p.Arg1438=)
c.3998_4025delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA (p.Arg1333=)
c.1895_1922delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA (p.Arg632=)
c.4337_4364delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA (p.Arg1446=)
c.4328_4355delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA (p.Arg1443=)
c.4319_4346delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA (p.Arg1440=)
c.2657_2684delinsGTGGTTTGGATGGTCCCCCTGGTCCAGA (p.Arg886=)
Xg.108687492_108687518delCA334058980COL4A5c.4326_4352del (p.Leu1443_Gly1451del)
c.4308_4334del (p.Leu1437_Gly1445del)
n.820_846del
c.122_148del
c.4317_4343del (p.Leu1440_Gly1448del)
c.4002_4028del (p.Leu1335_Gly1343del)
c.1899_1925del (p.Leu634_Gly642del)
c.4341_4367del (p.Leu1448_Gly1456del)
c.4332_4358del (p.Leu1445_Gly1453del)
c.4323_4349del (p.Leu1442_Gly1450del)
c.2661_2687del (p.Leu888_Gly896del)
dbSNP
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.108687507_108687534delinsTGGTCCAGATGGATTGCAAGGTCCCCCACA2450719217COL4A5c.4341_4368delinsTGGTCCAGATGGATTGCAAGGTCCCCCA (p.Pro1447=)
c.4323_4350delinsTGGTCCAGATGGATTGCAAGGTCCCCCA (p.Pro1441=)
n.835_862delinsTGGTCCAGATGGATTGCAAGGTCCCCCA
c.137_164delinsTGGTCCAGATGGATTGCAAGGTCCCCCA
c.4332_4359delinsTGGTCCAGATGGATTGCAAGGTCCCCCA (p.Pro1444=)
c.4017_4044delinsTGGTCCAGATGGATTGCAAGGTCCCCCA (p.Pro1339=)
c.1914_1941delinsTGGTCCAGATGGATTGCAAGGTCCCCCA (p.Pro638=)
c.4356_4383delinsTGGTCCAGATGGATTGCAAGGTCCCCCA (p.Pro1452=)
c.4347_4374delinsTGGTCCAGATGGATTGCAAGGTCCCCCA (p.Pro1449=)
c.4338_4365delinsTGGTCCAGATGGATTGCAAGGTCCCCCA (p.Pro1446=)
c.2676_2703delinsTGGTCCAGATGGATTGCAAGGTCCCCCA (p.Pro892=)
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.108687513A>CCA517924440COL4A5c.4347A>C (p.Pro1449=)
c.4329A>C (p.Pro1443=)
n.841A>C
c.143A>C
c.4338A>C (p.Pro1446=)
c.4023A>C (p.Pro1341=)
c.1920A>C (p.Pro640=)
c.4362A>C (p.Pro1454=)
c.4353A>C (p.Pro1451=)
c.4344A>C (p.Pro1448=)
c.2682A>C (p.Pro894=)
Xg.108687513A>GCA517924442COL4A5c.4347A>G (p.Pro1449=)
c.4329A>G (p.Pro1443=)
n.841A>G
c.143A>G
c.4338A>G (p.Pro1446=)
c.4023A>G (p.Pro1341=)
c.1920A>G (p.Pro640=)
c.4362A>G (p.Pro1454=)
c.4353A>G (p.Pro1451=)
c.4344A>G (p.Pro1448=)
c.2682A>G (p.Pro894=)
Xg.108687513A>TCA517924444COL4A5c.4347A>T (p.Pro1449=)
c.4329A>T (p.Pro1443=)
n.841A>T
c.143A>T
c.4338A>T (p.Pro1446=)
c.4023A>T (p.Pro1341=)
c.1920A>T (p.Pro640=)
c.4362A>T (p.Pro1454=)
c.4353A>T (p.Pro1451=)
c.4344A>T (p.Pro1448=)
c.2682A>T (p.Pro894=)
Xg.108687514G>ACA413854002COL4A5c.4348G>A (p.Asp1450Asn)
c.4330G>A (p.Asp1444Asn)
n.842G>A
c.144G>A
c.4339G>A (p.Asp1447Asn)
c.4024G>A (p.Asp1342Asn)
c.1921G>A (p.Asp641Asn)
c.4363G>A (p.Asp1455Asn)
c.4354G>A (p.Asp1452Asn)
c.4345G>A (p.Asp1449Asn)
c.2683G>A (p.Asp895Asn)
Xg.108687514G>CCA413854003COL4A5c.4348G>C (p.Asp1450His)
c.4330G>C (p.Asp1444His)
n.842G>C
c.144G>C
c.4339G>C (p.Asp1447His)
c.4024G>C (p.Asp1342His)
c.1921G>C (p.Asp641His)
c.4363G>C (p.Asp1455His)
c.4354G>C (p.Asp1452His)
c.4345G>C (p.Asp1449His)
c.2683G>C (p.Asp895His)
Xg.108687514G>TCA413854005COL4A5c.4348G>T (p.Asp1450Tyr)
c.4330G>T (p.Asp1444Tyr)
n.842G>T
c.144G>T
c.4339G>T (p.Asp1447Tyr)
c.4024G>T (p.Asp1342Tyr)
c.1921G>T (p.Asp641Tyr)
c.4363G>T (p.Asp1455Tyr)
c.4354G>T (p.Asp1452Tyr)
c.4345G>T (p.Asp1449Tyr)
c.2683G>T (p.Asp895Tyr)
Xg.108687515A>CCA413854010COL4A5c.4349A>C (p.Asp1450Ala)
c.4331A>C (p.Asp1444Ala)
n.843A>C
c.145A>C
c.4340A>C (p.Asp1447Ala)
c.4025A>C (p.Asp1342Ala)
c.1922A>C (p.Asp641Ala)
c.4364A>C (p.Asp1455Ala)
c.4355A>C (p.Asp1452Ala)
c.4346A>C (p.Asp1449Ala)
c.2684A>C (p.Asp895Ala)
Xg.108687515A>GCA413854008COL4A5c.4349A>G (p.Asp1450Gly)
c.4331A>G (p.Asp1444Gly)
n.843A>G
c.145A>G
c.4340A>G (p.Asp1447Gly)
c.4025A>G (p.Asp1342Gly)
c.1922A>G (p.Asp641Gly)
c.4364A>G (p.Asp1455Gly)
c.4355A>G (p.Asp1452Gly)
c.4346A>G (p.Asp1449Gly)
c.2684A>G (p.Asp895Gly)
Xg.108687515A>TCA413854007COL4A5c.4349A>T (p.Asp1450Val)
c.4331A>T (p.Asp1444Val)
n.843A>T
c.145A>T
c.4340A>T (p.Asp1447Val)
c.4025A>T (p.Asp1342Val)
c.1922A>T (p.Asp641Val)
c.4364A>T (p.Asp1455Val)
c.4355A>T (p.Asp1452Val)
c.4346A>T (p.Asp1449Val)
c.2684A>T (p.Asp895Val)
Xg.108687516T>ACA413854014COL4A5c.4350T>A (p.Asp1450Glu)
c.4332T>A (p.Asp1444Glu)
n.844T>A
c.146T>A
c.4341T>A (p.Asp1447Glu)
c.4026T>A (p.Asp1342Glu)
c.1923T>A (p.Asp641Glu)
c.4365T>A (p.Asp1455Glu)
c.4356T>A (p.Asp1452Glu)
c.4347T>A (p.Asp1449Glu)
c.2685T>A (p.Asp895Glu)
Xg.108687516T>CCA517924448COL4A5c.4350T>C (p.Asp1450=)
c.4332T>C (p.Asp1444=)
n.844T>C
c.146T>C
c.4341T>C (p.Asp1447=)
c.4026T>C (p.Asp1342=)
c.1923T>C (p.Asp641=)
c.4365T>C (p.Asp1455=)
c.4356T>C (p.Asp1452=)
c.4347T>C (p.Asp1449=)
c.2685T>C (p.Asp895=)
dbSNP gnomAD v2 gnomAD v4
Xg.108687516T>GCA413854012COL4A5c.4350T>G (p.Asp1450Glu)
c.4332T>G (p.Asp1444Glu)
n.844T>G
c.146T>G
c.4341T>G (p.Asp1447Glu)
c.4026T>G (p.Asp1342Glu)
c.1923T>G (p.Asp641Glu)
c.4365T>G (p.Asp1455Glu)
c.4356T>G (p.Asp1452Glu)
c.4347T>G (p.Asp1449Glu)
c.2685T>G (p.Asp895Glu)
Xg.108687516T=CA2450719228COL4A5c.4350T= (p.Asp1450=)
c.4332T= (p.Asp1444=)
n.844T=
c.146T=
c.4341T= (p.Asp1447=)
c.4026T= (p.Asp1342=)
c.1923T= (p.Asp641=)
c.4365T= (p.Asp1455=)
c.4356T= (p.Asp1452=)
c.4347T= (p.Asp1449=)
c.2685T= (p.Asp895=)
Xg.108687517G>ACA413854017COL4A5c.4351G>A (p.Gly1451Arg)
c.4333G>A (p.Gly1445Arg)
n.845G>A
c.147G>A
c.4342G>A (p.Gly1448Arg)
c.4027G>A (p.Gly1343Arg)
c.1924G>A (p.Gly642Arg)
c.4366G>A (p.Gly1456Arg)
c.4357G>A (p.Gly1453Arg)
c.4348G>A (p.Gly1450Arg)
c.2686G>A (p.Gly896Arg)
Xg.108687517G>CCA413854019COL4A5c.4351G>C (p.Gly1451Arg)
c.4333G>C (p.Gly1445Arg)
n.845G>C
c.147G>C
c.4342G>C (p.Gly1448Arg)
c.4027G>C (p.Gly1343Arg)
c.1924G>C (p.Gly642Arg)
c.4366G>C (p.Gly1456Arg)
c.4357G>C (p.Gly1453Arg)
c.4348G>C (p.Gly1450Arg)
c.2686G>C (p.Gly896Arg)
Xg.108687517G>TCA413854020COL4A5c.4351G>T (p.Gly1451Ter)
c.4333G>T (p.Gly1445Ter)
n.845G>T
c.147G>T
c.4342G>T (p.Gly1448Ter)
c.4027G>T (p.Gly1343Ter)
c.1924G>T (p.Gly642Ter)
c.4366G>T (p.Gly1456Ter)
c.4357G>T (p.Gly1453Ter)
c.4348G>T (p.Gly1450Ter)
c.2686G>T (p.Gly896Ter)
Xg.108687518G>ACA413854022COL4A5c.4352G>A (p.Gly1451Glu)
c.4334G>A (p.Gly1445Glu)
n.846G>A
c.148G>A
c.4343G>A (p.Gly1448Glu)
c.4028G>A (p.Gly1343Glu)
c.1925G>A (p.Gly642Glu)
c.4367G>A (p.Gly1456Glu)
c.4358G>A (p.Gly1453Glu)
c.4349G>A (p.Gly1450Glu)
c.2687G>A (p.Gly896Glu)
ClinVar
Xg.108687518G>CCA413854024COL4A5c.4352G>C (p.Gly1451Ala)
c.4334G>C (p.Gly1445Ala)
n.846G>C
c.148G>C
c.4343G>C (p.Gly1448Ala)
c.4028G>C (p.Gly1343Ala)
c.1925G>C (p.Gly642Ala)
c.4367G>C (p.Gly1456Ala)
c.4358G>C (p.Gly1453Ala)
c.4349G>C (p.Gly1450Ala)
c.2687G>C (p.Gly896Ala)
Xg.108687518G>TCA413854026COL4A5c.4352G>T (p.Gly1451Val)
c.4334G>T (p.Gly1445Val)
n.846G>T
c.148G>T
c.4343G>T (p.Gly1448Val)
c.4028G>T (p.Gly1343Val)
c.1925G>T (p.Gly642Val)
c.4367G>T (p.Gly1456Val)
c.4358G>T (p.Gly1453Val)
c.4349G>T (p.Gly1450Val)
c.2687G>T (p.Gly896Val)
Xg.108687519A=CA2450719234COL4A5c.4353A= (p.Gly1451=)
c.4335A= (p.Gly1445=)
n.847A=
c.149A=
c.4344A= (p.Gly1448=)
c.4029A= (p.Gly1343=)
c.1926A= (p.Gly642=)
c.4368A= (p.Gly1456=)
c.4359A= (p.Gly1453=)
c.4350A= (p.Gly1450=)
c.2688A= (p.Gly896=)
Xg.108687519A>CCA517924453COL4A5c.4353A>C (p.Gly1451=)
c.4335A>C (p.Gly1445=)
n.847A>C
c.149A>C
c.4344A>C (p.Gly1448=)
c.4029A>C (p.Gly1343=)
c.1926A>C (p.Gly642=)
c.4368A>C (p.Gly1456=)
c.4359A>C (p.Gly1453=)
c.4350A>C (p.Gly1450=)
c.2688A>C (p.Gly896=)
Xg.108687519A>GCA517924455COL4A5c.4353A>G (p.Gly1451=)
c.4335A>G (p.Gly1445=)
n.847A>G
c.149A>G
c.4344A>G (p.Gly1448=)
c.4029A>G (p.Gly1343=)
c.1926A>G (p.Gly642=)
c.4368A>G (p.Gly1456=)
c.4359A>G (p.Gly1453=)
c.4350A>G (p.Gly1450=)
c.2688A>G (p.Gly896=)
ClinVar gnomAD v4
Xg.108687519A>TCA10489348COL4A5c.4353A>T (p.Gly1451=)
c.4335A>T (p.Gly1445=)
n.847A>T
c.149A>T
c.4344A>T (p.Gly1448=)
c.4029A>T (p.Gly1343=)
c.1926A>T (p.Gly642=)
c.4368A>T (p.Gly1456=)
c.4359A>T (p.Gly1453=)
c.4350A>T (p.Gly1450=)
c.2688A>T (p.Gly896=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.108687520T>ACA413854029COL4A5c.4354T>A (p.Leu1452Met)
c.4336T>A (p.Leu1446Met)
n.848T>A
c.150T>A
c.4345T>A (p.Leu1449Met)
c.4030T>A (p.Leu1344Met)
c.1927T>A (p.Leu643Met)
c.4369T>A (p.Leu1457Met)
c.4360T>A (p.Leu1454Met)
c.4351T>A (p.Leu1451Met)
c.2689T>A (p.Leu897Met)
Xg.108687520T>CCA517924457COL4A5c.4354T>C (p.Leu1452=)
c.4336T>C (p.Leu1446=)
n.848T>C
c.150T>C
c.4345T>C (p.Leu1449=)
c.4030T>C (p.Leu1344=)
c.1927T>C (p.Leu643=)
c.4369T>C (p.Leu1457=)
c.4360T>C (p.Leu1454=)
c.4351T>C (p.Leu1451=)
c.2689T>C (p.Leu897=)
Xg.108687520T>GCA413854031COL4A5c.4354T>G (p.Leu1452Val)
c.4336T>G (p.Leu1446Val)
n.848T>G
c.150T>G
c.4345T>G (p.Leu1449Val)
c.4030T>G (p.Leu1344Val)
c.1927T>G (p.Leu643Val)
c.4369T>G (p.Leu1457Val)
c.4360T>G (p.Leu1454Val)
c.4351T>G (p.Leu1451Val)
c.2689T>G (p.Leu897Val)
dbSNP gnomAD v4
Xg.108687520T=CA2450719235COL4A5c.4354T= (p.Leu1452=)
c.4336T= (p.Leu1446=)
n.848T=
c.150T=
c.4345T= (p.Leu1449=)
c.4030T= (p.Leu1344=)
c.1927T= (p.Leu643=)
c.4369T= (p.Leu1457=)
c.4360T= (p.Leu1454=)
c.4351T= (p.Leu1451=)
c.2689T= (p.Leu897=)
Xg.108687521T>ACA413854033COL4A5c.4355T>A (p.Leu1452Ter)
c.4337T>A (p.Leu1446Ter)
n.849T>A
c.151T>A
c.4346T>A (p.Leu1449Ter)
c.4031T>A (p.Leu1344Ter)
c.1928T>A (p.Leu643Ter)
c.4370T>A (p.Leu1457Ter)
c.4361T>A (p.Leu1454Ter)
c.4352T>A (p.Leu1451Ter)
c.2690T>A (p.Leu897Ter)
Xg.108687521T>CCA413854035COL4A5c.4355T>C (p.Leu1452Ser)
c.4337T>C (p.Leu1446Ser)
n.849T>C
c.151T>C
c.4346T>C (p.Leu1449Ser)
c.4031T>C (p.Leu1344Ser)
c.1928T>C (p.Leu643Ser)
c.4370T>C (p.Leu1457Ser)
c.4361T>C (p.Leu1454Ser)
c.4352T>C (p.Leu1451Ser)
c.2690T>C (p.Leu897Ser)
gnomAD v4
Xg.108687521T>GCA413854038COL4A5c.4355T>G (p.Leu1452Trp)
c.4337T>G (p.Leu1446Trp)
n.849T>G
c.151T>G
c.4346T>G (p.Leu1449Trp)
c.4031T>G (p.Leu1344Trp)
c.1928T>G (p.Leu643Trp)
c.4370T>G (p.Leu1457Trp)
c.4361T>G (p.Leu1454Trp)
c.4352T>G (p.Leu1451Trp)
c.2690T>G (p.Leu897Trp)
Xg.108687522G>ACA517924461COL4A5c.4356G>A (p.Leu1452=)
c.4338G>A (p.Leu1446=)
n.850G>A
c.152G>A
c.4347G>A (p.Leu1449=)
c.4032G>A (p.Leu1344=)
c.1929G>A (p.Leu643=)
c.4371G>A (p.Leu1457=)
c.4362G>A (p.Leu1454=)
c.4353G>A (p.Leu1451=)
c.2691G>A (p.Leu897=)
Xg.108687522G>CCA413854041COL4A5c.4356G>C (p.Leu1452Phe)
c.4338G>C (p.Leu1446Phe)
n.850G>C
c.152G>C
c.4347G>C (p.Leu1449Phe)
c.4032G>C (p.Leu1344Phe)
c.1929G>C (p.Leu643Phe)
c.4371G>C (p.Leu1457Phe)
c.4362G>C (p.Leu1454Phe)
c.4353G>C (p.Leu1451Phe)
c.2691G>C (p.Leu897Phe)
Xg.108687522G>TCA413854040COL4A5c.4356G>T (p.Leu1452Phe)
c.4338G>T (p.Leu1446Phe)
n.850G>T
c.152G>T
c.4347G>T (p.Leu1449Phe)
c.4032G>T (p.Leu1344Phe)
c.1929G>T (p.Leu643Phe)
c.4371G>T (p.Leu1457Phe)
c.4362G>T (p.Leu1454Phe)
c.4353G>T (p.Leu1451Phe)
c.2691G>T (p.Leu897Phe)
Xg.108687523C>ACA413854044COL4A5c.4357C>A (p.Gln1453Lys)
c.4339C>A (p.Gln1447Lys)
n.851C>A
c.153C>A
c.4348C>A (p.Gln1450Lys)
c.4033C>A (p.Gln1345Lys)
c.1930C>A (p.Gln644Lys)
c.4372C>A (p.Gln1458Lys)
c.4363C>A (p.Gln1455Lys)
c.4354C>A (p.Gln1452Lys)
c.2692C>A (p.Gln898Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.108687523C=CA2450719237COL4A5c.4357C= (p.Gln1453=)
c.4339C= (p.Gln1447=)
n.851C=
c.153C=
c.4348C= (p.Gln1450=)
c.4033C= (p.Gln1345=)
c.1930C= (p.Gln644=)
c.4372C= (p.Gln1458=)
c.4363C= (p.Gln1455=)
c.4354C= (p.Gln1452=)
c.2692C= (p.Gln898=)
Xg.108687523C>GCA413854046COL4A5c.4357C>G (p.Gln1453Glu)
c.4339C>G (p.Gln1447Glu)
n.851C>G
c.153C>G
c.4348C>G (p.Gln1450Glu)
c.4033C>G (p.Gln1345Glu)
c.1930C>G (p.Gln644Glu)
c.4372C>G (p.Gln1458Glu)
c.4363C>G (p.Gln1455Glu)
c.4354C>G (p.Gln1452Glu)
c.2692C>G (p.Gln898Glu)
Xg.108687523C>TCA413854047COL4A5c.4357C>T (p.Gln1453Ter)
c.4339C>T (p.Gln1447Ter)
n.851C>T
c.153C>T
c.4348C>T (p.Gln1450Ter)
c.4033C>T (p.Gln1345Ter)
c.1930C>T (p.Gln644Ter)
c.4372C>T (p.Gln1458Ter)
c.4363C>T (p.Gln1455Ter)
c.4354C>T (p.Gln1452Ter)
c.2692C>T (p.Gln898Ter)
Xg.108687524A>CCA413854048COL4A5c.4358A>C (p.Gln1453Pro)
c.4340A>C (p.Gln1447Pro)
n.852A>C
c.154A>C
c.4349A>C (p.Gln1450Pro)
c.4034A>C (p.Gln1345Pro)
c.1931A>C (p.Gln644Pro)
c.4373A>C (p.Gln1458Pro)
c.4364A>C (p.Gln1455Pro)
c.4355A>C (p.Gln1452Pro)
c.2693A>C (p.Gln898Pro)
Xg.108687524A>GCA413854049COL4A5c.4358A>G (p.Gln1453Arg)
c.4340A>G (p.Gln1447Arg)
n.852A>G
c.154A>G
c.4349A>G (p.Gln1450Arg)
c.4034A>G (p.Gln1345Arg)
c.1931A>G (p.Gln644Arg)
c.4373A>G (p.Gln1458Arg)
c.4364A>G (p.Gln1455Arg)
c.4355A>G (p.Gln1452Arg)
c.2693A>G (p.Gln898Arg)
Xg.108687524A>TCA413854052COL4A5c.4358A>T (p.Gln1453Leu)
c.4340A>T (p.Gln1447Leu)
n.852A>T
c.154A>T
c.4349A>T (p.Gln1450Leu)
c.4034A>T (p.Gln1345Leu)
c.1931A>T (p.Gln644Leu)
c.4373A>T (p.Gln1458Leu)
c.4364A>T (p.Gln1455Leu)
c.4355A>T (p.Gln1452Leu)
c.2693A>T (p.Gln898Leu)
Xg.108687525A>CCA413854054COL4A5c.4359A>C (p.Gln1453His)
c.4341A>C (p.Gln1447His)
n.853A>C
c.155A>C
c.4350A>C (p.Gln1450His)
c.4035A>C (p.Gln1345His)
c.1932A>C (p.Gln644His)
c.4374A>C (p.Gln1458His)
c.4365A>C (p.Gln1455His)
c.4356A>C (p.Gln1452His)
c.2694A>C (p.Gln898His)
Xg.108687525A>GCA517924465COL4A5c.4359A>G (p.Gln1453=)
c.4341A>G (p.Gln1447=)
n.853A>G
c.155A>G
c.4350A>G (p.Gln1450=)
c.4035A>G (p.Gln1345=)
c.1932A>G (p.Gln644=)
c.4374A>G (p.Gln1458=)
c.4365A>G (p.Gln1455=)
c.4356A>G (p.Gln1452=)
c.2694A>G (p.Gln898=)
Xg.108687525A>TCA413854056COL4A5c.4359A>T (p.Gln1453His)
c.4341A>T (p.Gln1447His)
n.853A>T
c.155A>T
c.4350A>T (p.Gln1450His)
c.4035A>T (p.Gln1345His)
c.1932A>T (p.Gln644His)
c.4374A>T (p.Gln1458His)
c.4365A>T (p.Gln1455His)
c.4356A>T (p.Gln1452His)
c.2694A>T (p.Gln898His)
Xg.108687526G>ACA259040COL4A5c.4360G>A (p.Gly1454Ser)
c.4342G>A (p.Gly1448Ser)
n.854G>A
c.156G>A
c.4351G>A (p.Gly1451Ser)
c.4036G>A (p.Gly1346Ser)
c.1933G>A (p.Gly645Ser)
c.4375G>A (p.Gly1459Ser)
c.4366G>A (p.Gly1456Ser)
c.4357G>A (p.Gly1453Ser)
c.2695G>A (p.Gly899Ser)
ClinVar dbSNP
Xg.108687526G>CCA413854059COL4A5c.4360G>C (p.Gly1454Arg)
c.4342G>C (p.Gly1448Arg)
n.854G>C
c.156G>C
c.4351G>C (p.Gly1451Arg)
c.4036G>C (p.Gly1346Arg)
c.1933G>C (p.Gly645Arg)
c.4375G>C (p.Gly1459Arg)
c.4366G>C (p.Gly1456Arg)
c.4357G>C (p.Gly1453Arg)
c.2695G>C (p.Gly899Arg)
ClinVar gnomAD v4

Number of alleles fetched