Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32435082_32435084dupCA2580615657WT1c.286_288dup (p.Gly96_Cys97insGly)
c.271_273dup (p.Gly91_Cys92insGly)
n.465_467dup
ClinVar dbSNP gnomAD v4
11g.32435082_32435084delCA064802WT1c.286_288del (p.Gly96del)
c.271_273del (p.Gly91del)
n.465_467del
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435077C>ACA379966004WT1c.284G>T (p.Gly95Val)
c.269G>T (p.Gly90Val)
n.463G>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435077C=CA1962327320WT1c.284G= (p.Gly95=)
c.269G= (p.Gly90=)
n.463G=
11g.32435077C>GCA379966005WT1c.284G>C (p.Gly95Ala)
c.269G>C (p.Gly90Ala)
n.463G>C
dbSNP
11g.32435077C>TCA379966006WT1c.284G>A (p.Gly95Asp)
c.269G>A (p.Gly90Asp)
n.463G>A
ClinVar dbSNP gnomAD v4
11g.32435078C>ACA379966007WT1c.283G>T (p.Gly95Cys)
c.268G>T (p.Gly90Cys)
n.462G>T
gnomAD v4
11g.32435078C>GCA379966008WT1c.283G>C (p.Gly95Arg)
c.268G>C (p.Gly90Arg)
n.462G>C
dbSNP gnomAD v4
11g.32435078C>TCA379966009WT1c.283G>A (p.Gly95Ser)
c.268G>A (p.Gly90Ser)
n.462G>A
dbSNP gnomAD v4
11g.32435079G>ACA473773952WT1c.282C>T (p.Gly94=)
c.267C>T (p.Gly89=)
n.461C>T
ClinVar dbSNP gnomAD v4
11g.32435079G>CCA473773953WT1c.282C>G (p.Gly94=)
c.267C>G (p.Gly89=)
n.461C>G
dbSNP
11g.32435079G=CA1962327321WT1c.282C= (p.Gly94=)
c.267C= (p.Gly89=)
n.461C=
11g.32435079G>TCA473773954WT1c.282C>A (p.Gly94=)
c.267C>A (p.Gly89=)
n.461C>A
gnomAD v4
11g.32435080C>ACA379966012WT1c.281G>T (p.Gly94Val)
c.266G>T (p.Gly89Val)
n.460G>T
gnomAD v4
11g.32435080C=CA1962327322WT1c.281G= (p.Gly94=)
c.266G= (p.Gly89=)
n.460G=
11g.32435080C>GCA379966011WT1c.281G>C (p.Gly94Ala)
c.266G>C (p.Gly89Ala)
n.460G>C
11g.32435080C>TCA379966010WT1c.281G>A (p.Gly94Asp)
c.266G>A (p.Gly89Asp)
n.460G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435081C>ACA379966014WT1c.280G>T (p.Gly94Cys)
c.265G>T (p.Gly89Cys)
n.459G>T
gnomAD v4
11g.32435081C=CA1962327323WT1c.280G= (p.Gly94=)
c.265G= (p.Gly89=)
n.459G=
11g.32435081C>GCA379966013WT1c.280G>C (p.Gly94Arg)
c.265G>C (p.Gly89Arg)
n.459G>C
gnomAD v4
11g.32435081C>TCA064798WT1c.280G>A (p.Gly94Ser)
c.265G>A (p.Gly89Ser)
n.459G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435082G>ACA473773960WT1c.279C>T (p.Gly93=)
c.264C>T (p.Gly88=)
n.458C>T
ClinVar dbSNP gnomAD v4
11g.32435082G>CCA473773962WT1c.279C>G (p.Gly93=)
c.264C>G (p.Gly88=)
n.458C>G
dbSNP
11g.32435082G=CA1962327324WT1c.279C= (p.Gly93=)
c.264C= (p.Gly88=)
n.458C=
11g.32435082G>TCA473773961WT1c.279C>A (p.Gly93=)
c.264C>A (p.Gly88=)
n.458C>A
ClinVar dbSNP gnomAD v4
11g.32435084_32435112delCA2695213680WT1c.251_279del (p.Leu84ArgfsTer?)
c.236_264del (p.Leu79ArgfsTer?)
n.430_458del
11g.32435083C>ACA379966015WT1c.278G>T (p.Gly93Val)
c.263G>T (p.Gly88Val)
n.457G>T
gnomAD v4
11g.32435083C=CA1962327325WT1c.278G= (p.Gly93=)
c.263G= (p.Gly88=)
n.457G=
11g.32435083C>GCA379966016WT1c.278G>C (p.Gly93Ala)
c.263G>C (p.Gly88Ala)
n.457G>C
ClinVar dbSNP gnomAD v4
11g.32435083C>TCA379966017WT1c.278G>A (p.Gly93Asp)
c.263G>A (p.Gly88Asp)
n.457G>A
ClinVar dbSNP gnomAD v4
11g.32435085_32435087delCA2612989581WT1c.276_278del (p.Gly93del)
c.261_263del (p.Gly88del)
n.455_457del
gnomAD v4
11g.32435084C>ACA379966020WT1c.277G>T (p.Gly93Cys)
c.262G>T (p.Gly88Cys)
n.456G>T
gnomAD v4
11g.32435084C>GCA379966019WT1c.277G>C (p.Gly93Arg)
c.262G>C (p.Gly88Arg)
n.456G>C
11g.32435084C>TCA379966018WT1c.277G>A (p.Gly93Ser)
c.262G>A (p.Gly88Ser)
n.456G>A
gnomAD v4
11g.32435085delCA2573146230WT1c.276del (p.Gly93AlafsTer9)
c.261del (p.Gly88AlafsTer9)
n.455del
ClinVar dbSNP
11g.32435085A>CCA473773968WT1c.276T>G (p.Gly92=)
c.261T>G (p.Gly87=)
n.455T>G
dbSNP
11g.32435085A>GCA473773970WT1c.276T>C (p.Gly92=)
c.261T>C (p.Gly87=)
n.455T>C
gnomAD v4
11g.32435085A>TCA473773972WT1c.276T>A (p.Gly92=)
c.261T>A (p.Gly87=)
n.455T>A
11g.32435086C>ACA379966021WT1c.275G>T (p.Gly92Val)
c.260G>T (p.Gly87Val)
n.454G>T
gnomAD v4
11g.32435086C>GCA379966022WT1c.275G>C (p.Gly92Ala)
c.260G>C (p.Gly87Ala)
n.454G>C
11g.32435086C>TCA379966023WT1c.275G>A (p.Gly92Asp)
c.260G>A (p.Gly87Asp)
n.454G>A
ClinVar
11g.32435088dupCA2740093680WT1c.275dup (p.Gly93TrpfsTer?)
c.260dup (p.Gly88TrpfsTer?)
n.454dup
ClinVar
11g.32435088delCA2612989583WT1c.275del (p.Gly92ValfsTer10)
c.260del (p.Gly87ValfsTer10)
n.454del
gnomAD v4
11g.32435087C>ACA379966024WT1c.274G>T (p.Gly92Cys)
c.259G>T (p.Gly87Cys)
n.453G>T
gnomAD v4
11g.32435087C>GCA379966025WT1c.274G>C (p.Gly92Arg)
c.259G>C (p.Gly87Arg)
n.453G>C
11g.32435087C>TCA379966026WT1c.274G>A (p.Gly92Ser)
c.259G>A (p.Gly87Ser)
n.453G>A
gnomAD v4
11g.32435088C>ACA473773977WT1c.273G>T (p.Leu91=)
c.258G>T (p.Leu86=)
n.452G>T
dbSNP gnomAD v4
11g.32435088C=CA1962327326WT1c.273G= (p.Leu91=)
c.258G= (p.Leu86=)
n.452G=
11g.32435088C>GCA473773978WT1c.273G>C (p.Leu91=)
c.258G>C (p.Leu86=)
n.452G>C
11g.32435088C>TCA473773980WT1c.273G>A (p.Leu91=)
c.258G>A (p.Leu86=)
n.452G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435089A>CCA379966027WT1c.272T>G (p.Leu91Arg)
c.257T>G (p.Leu86Arg)
n.451T>G
11g.32435089A>GCA379966029WT1c.272T>C (p.Leu91Pro)
c.257T>C (p.Leu86Pro)
n.451T>C
gnomAD v4
11g.32435089A>TCA379966028WT1c.272T>A (p.Leu91Gln)
c.257T>A (p.Leu86Gln)
n.451T>A
gnomAD v4
11g.32435090G>ACA473773984WT1c.271C>T (p.Leu91=)
c.256C>T (p.Leu86=)
n.450C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435090G>CCA379966030WT1c.271C>G (p.Leu91Val)
c.256C>G (p.Leu86Val)
n.450C>G
dbSNP
11g.32435090G=CA1962327327WT1c.271C= (p.Leu91=)
c.256C= (p.Leu86=)
n.450C=
11g.32435090G>TCA379966031WT1c.271C>A (p.Leu91Met)
c.256C>A (p.Leu86Met)
n.450C>A
gnomAD v4
11g.32435094_32435098delCA645584492WT1c.267_271del (p.Ser90GlyfsTer?)
c.252_256del (p.Ser85GlyfsTer?)
n.446_450del
COSMIC COSMIC
11g.32435091G>ACA473773986WT1c.270C>T (p.Ser90=)
c.255C>T (p.Ser85=)
n.449C>T
ClinVar dbSNP gnomAD v4
11g.32435091G>CCA064793WT1c.270C>G (p.Ser90=)
c.255C>G (p.Ser85=)
n.449C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435091G=CA1962327328WT1c.270C= (p.Ser90=)
c.255C= (p.Ser85=)
n.449C=
11g.32435091G>TCA473773987WT1c.270C>A (p.Ser90=)
c.255C>A (p.Ser85=)
n.449C>A
gnomAD v4
11g.32435092G>ACA379966032WT1c.269C>T (p.Ser90Phe)
c.254C>T (p.Ser85Phe)
n.448C>T
ClinVar dbSNP gnomAD v4
11g.32435092G>CCA379966033WT1c.269C>G (p.Ser90Cys)
c.254C>G (p.Ser85Cys)
n.448C>G
11g.32435092G=CA1962327329WT1c.269C= (p.Ser90=)
c.254C= (p.Ser85=)
n.448C=
11g.32435092G>TCA379966034WT1c.269C>A (p.Ser90Tyr)
c.254C>A (p.Ser85Tyr)
n.448C>A
gnomAD v4
11g.32435093A=CA1962327330WT1c.268T= (p.Ser90=)
c.253T= (p.Ser85=)
n.447T=
11g.32435093A>CCA379966035WT1c.268T>G (p.Ser90Ala)
c.253T>G (p.Ser85Ala)
n.447T>G
11g.32435093A>GCA379966036WT1c.268T>C (p.Ser90Pro)
c.253T>C (p.Ser85Pro)
n.447T>C
ClinVar dbSNP gnomAD v4
11g.32435093A>TCA379966037WT1c.268T>A (p.Ser90Thr)
c.253T>A (p.Ser85Thr)
n.447T>A
11g.32435094G>ACA473773990WT1c.267C>T (p.Pro89=)
c.252C>T (p.Pro84=)
n.446C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435094G>CCA473773995WT1c.267C>G (p.Pro89=)
c.252C>G (p.Pro84=)
n.446C>G
gnomAD v4
11g.32435094G=CA1962327331WT1c.267C= (p.Pro89=)
c.252C= (p.Pro84=)
n.446C=
11g.32435094G>TCA473773996WT1c.267C>A (p.Pro89=)
c.252C>A (p.Pro84=)
n.446C>A
gnomAD v4
11g.32435095G>ACA379966038WT1c.266C>T (p.Pro89Leu)
c.251C>T (p.Pro84Leu)
n.445C>T
ClinVar dbSNP gnomAD v4
11g.32435095G>CCA379966039WT1c.266C>G (p.Pro89Arg)
c.251C>G (p.Pro84Arg)
n.445C>G
ClinVar
11g.32435095G=CA1962327332WT1c.266C= (p.Pro89=)
c.251C= (p.Pro84=)
n.445C=
11g.32435095G>TCA379966040WT1c.266C>A (p.Pro89His)
c.251C>A (p.Pro84His)
n.445C>A
gnomAD v4
11g.32435096G>ACA379966042WT1c.265C>T (p.Pro89Ser)
c.250C>T (p.Pro84Ser)
n.444C>T
gnomAD v4
11g.32435096G>CCA379966043WT1c.265C>G (p.Pro89Ala)
c.250C>G (p.Pro84Ala)
n.444C>G
dbSNP
11g.32435096G>TCA379966041WT1c.265C>A (p.Pro89Thr)
c.250C>A (p.Pro84Thr)
n.444C>A
ClinVar gnomAD v4 COSMIC COSMIC
11g.32435096_32435098delCA2574790568WT1c.263_265del (p.Val88_Pro89delinsAla)
c.248_250del (p.Val83_Pro84delinsAla)
n.442_444del
11g.32435097G>ACA473774000WT1c.264C>T (p.Val88=)
c.249C>T (p.Val83=)
n.443C>T
dbSNP gnomAD v2 gnomAD v4
11g.32435097G>CCA473774001WT1c.264C>G (p.Val88=)
c.249C>G (p.Val83=)
n.443C>G
gnomAD v4
11g.32435097G=CA1962327333WT1c.264C= (p.Val88=)
c.249C= (p.Val83=)
n.443C=
11g.32435097G>TCA473774003WT1c.264C>A (p.Val88=)
c.249C>A (p.Val83=)
n.443C>A
gnomAD v4
11g.32435098A>CCA379966044WT1c.263T>G (p.Val88Gly)
c.248T>G (p.Val83Gly)
n.442T>G
11g.32435098A>GCA379966045WT1c.263T>C (p.Val88Ala)
c.248T>C (p.Val83Ala)
n.442T>C
dbSNP gnomAD v4
11g.32435098A>TCA379966046WT1c.263T>A (p.Val88Asp)
c.248T>A (p.Val83Asp)
n.442T>A
ClinVar gnomAD v4
11g.32435099C>ACA379966047WT1c.262G>T (p.Val88Phe)
c.247G>T (p.Val83Phe)
n.441G>T
ClinVar dbSNP gnomAD v4
11g.32435099C=CA1962327334WT1c.262G= (p.Val88=)
c.247G= (p.Val83=)
n.441G=
11g.32435099C>GCA379966048WT1c.262G>C (p.Val88Leu)
c.247G>C (p.Val83Leu)
n.441G>C
gnomAD v4
11g.32435099C>TCA379966049WT1c.262G>A (p.Val88Ile)
c.247G>A (p.Val83Ile)
n.441G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435099_32435100delinsAACA2580084189WT1c.261_262delinsTT (p.Val88Phe)
c.246_247delinsTT (p.Val83Phe)
n.440_441delinsTT
ClinVar
11g.32435100G>ACA473774006WT1c.261C>T (p.Ala87=)
c.246C>T (p.Ala82=)
n.440C>T
ClinVar dbSNP gnomAD v4
11g.32435100G>CCA473774007WT1c.261C>G (p.Ala87=)
c.246C>G (p.Ala82=)
n.440C>G
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435100G=CA1962327335WT1c.261C= (p.Ala87=)
c.246C= (p.Ala82=)
n.440C=
11g.32435100G>TCA473774009WT1c.261C>A (p.Ala87=)
c.246C>A (p.Ala82=)
n.440C>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435101G>ACA379966052WT1c.260C>T (p.Ala87Val)
c.245C>T (p.Ala82Val)
n.439C>T
dbSNP gnomAD v4
11g.32435101G>CCA379966051WT1c.260C>G (p.Ala87Gly)
c.245C>G (p.Ala82Gly)
n.439C>G
11g.32435101G>TCA379966050WT1c.260C>A (p.Ala87Asp)
c.245C>A (p.Ala82Asp)
n.439C>A
11g.32435102C>ACA379966053WT1c.259G>T (p.Ala87Ser)
c.244G>T (p.Ala82Ser)
n.438G>T
gnomAD v4
11g.32435102C=CA1962327336WT1c.259G= (p.Ala87=)
c.244G= (p.Ala82=)
n.438G=
11g.32435102C>GCA379966054WT1c.259G>C (p.Ala87Pro)
c.244G>C (p.Ala82Pro)
n.438G>C
dbSNP gnomAD v4
11g.32435102C>TCA064789WT1c.259G>A (p.Ala87Thr)
c.244G>A (p.Ala82Thr)
n.438G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435103G>ACA473774014WT1c.258C>T (p.Pro86=)
c.243C>T (p.Pro81=)
n.437C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435103G>CCA473774015WT1c.258C>G (p.Pro86=)
c.243C>G (p.Pro81=)
n.437C>G
11g.32435103G=CA1962327337WT1c.258C= (p.Pro86=)
c.243C= (p.Pro81=)
n.437C=
11g.32435103G>TCA473774012WT1c.258C>A (p.Pro86=)
c.243C>A (p.Pro81=)
n.437C>A
ClinVar dbSNP gnomAD v4
11g.32435105_32435106insGCCCGGGCGCCTGGGCA2790963048WT1c.258_259insAGGCGCCCGGGCCCC (p.Pro86_Ala87insArgArgProGlyPro)
c.243_244insAGGCGCCCGGGCCCC (p.Pro81_Ala82insArgArgProGlyPro)
n.437_438insAGGCGCCCGGGCCCC
11g.32435104G>ACA379966055WT1c.257C>T (p.Pro86Leu)
c.242C>T (p.Pro81Leu)
n.436C>T
ClinVar gnomAD v4
11g.32435104G>CCA379966056WT1c.257C>G (p.Pro86Arg)
c.242C>G (p.Pro81Arg)
n.436C>G
11g.32435104G>TCA379966057WT1c.257C>A (p.Pro86His)
c.242C>A (p.Pro81His)
n.436C>A
gnomAD v4
11g.32435105G>ACA379966058WT1c.256C>T (p.Pro86Ser)
c.241C>T (p.Pro81Ser)
n.435C>T
dbSNP gnomAD v4 COSMIC COSMIC
11g.32435105G>CCA379966060WT1c.256C>G (p.Pro86Ala)
c.241C>G (p.Pro81Ala)
n.435C>G
11g.32435105G>TCA379966059WT1c.256C>A (p.Pro86Thr)
c.241C>A (p.Pro81Thr)
n.435C>A
gnomAD v4
11g.32435106C>ACA473774031WT1c.255G>T (p.Leu85=)
c.240G>T (p.Leu80=)
n.434G>T
gnomAD v4
11g.32435106C=CA1962327338WT1c.255G= (p.Leu85=)
c.240G= (p.Leu80=)
n.434G=
11g.32435106C>GCA473774024WT1c.255G>C (p.Leu85=)
c.240G>C (p.Leu80=)
n.434G>C
11g.32435106C>TCA473774023WT1c.255G>A (p.Leu85=)
c.240G>A (p.Leu80=)
n.434G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435107A>CCA379966061WT1c.254T>G (p.Leu85Arg)
c.239T>G (p.Leu80Arg)
n.433T>G
11g.32435107A>GCA379966062WT1c.254T>C (p.Leu85Pro)
c.239T>C (p.Leu80Pro)
n.433T>C
ClinVar gnomAD v4
11g.32435107A>TCA379966063WT1c.254T>A (p.Leu85Gln)
c.239T>A (p.Leu80Gln)
n.433T>A
gnomAD v4
11g.32435108G>ACA473774032WT1c.253C>T (p.Leu85=)
c.238C>T (p.Leu80=)
n.432C>T
dbSNP gnomAD v4
11g.32435108G>CCA379966064WT1c.253C>G (p.Leu85Val)
c.238C>G (p.Leu80Val)
n.432C>G
11g.32435108G>TCA379966065WT1c.253C>A (p.Leu85Met)
c.238C>A (p.Leu80Met)
n.432C>A
gnomAD v4
11g.32435109C>ACA473774035WT1c.252G>T (p.Leu84=)
c.237G>T (p.Leu79=)
n.431G>T
dbSNP gnomAD v2 gnomAD v4
11g.32435109C=CA1962327339WT1c.252G= (p.Leu84=)
c.237G= (p.Leu79=)
n.431G=
11g.32435109C>GCA473774038WT1c.252G>C (p.Leu84=)
c.237G>C (p.Leu79=)
n.431G>C
11g.32435109C>TCA473774037WT1c.252G>A (p.Leu84=)
c.237G>A (p.Leu79=)
n.431G>A
dbSNP gnomAD v4
11g.32435110A>CCA379966066WT1c.251T>G (p.Leu84Arg)
c.236T>G (p.Leu79Arg)
n.430T>G
gnomAD v4
11g.32435110A>GCA379966067WT1c.251T>C (p.Leu84Pro)
c.236T>C (p.Leu79Pro)
n.430T>C
gnomAD v4
11g.32435110A>TCA379966068WT1c.251T>A (p.Leu84Gln)
c.236T>A (p.Leu79Gln)
n.430T>A
11g.32435111G>ACA064783WT1c.250C>T (p.Leu84=)
c.235C>T (p.Leu79=)
n.429C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435111G>CCA379966069WT1c.250C>G (p.Leu84Val)
c.235C>G (p.Leu79Val)
n.429C>G
11g.32435111G=CA1962327340WT1c.250C= (p.Leu84=)
c.235C= (p.Leu79=)
n.429C=
11g.32435111G>TCA379966070WT1c.250C>A (p.Leu84Met)
c.235C>A (p.Leu79Met)
n.429C>A
gnomAD v4
11g.32435112C>ACA473774039WT1c.249G>T (p.Ala83=)
c.234G>T (p.Ala78=)
n.428G>T
ClinVar gnomAD v4
11g.32435112C=CA1962327341WT1c.249G= (p.Ala83=)
c.234G= (p.Ala78=)
n.428G=
11g.32435112C>GCA473774040WT1c.249G>C (p.Ala83=)
c.234G>C (p.Ala78=)
n.428G>C
dbSNP gnomAD v2 gnomAD v4
11g.32435112C>TCA473774041WT1c.249G>A (p.Ala83=)
c.234G>A (p.Ala78=)
n.428G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435113G>ACA379966071WT1c.248C>T (p.Ala83Val)
c.233C>T (p.Ala78Val)
n.427C>T
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
11g.32435113G>CCA379966073WT1c.248C>G (p.Ala83Gly)
c.233C>G (p.Ala78Gly)
n.427C>G
11g.32435113G=CA1962327342WT1c.248C= (p.Ala83=)
c.233C= (p.Ala78=)
n.427C=
11g.32435113G>TCA379966072WT1c.248C>A (p.Ala83Glu)
c.233C>A (p.Ala78Glu)
n.427C>A
gnomAD v4
11g.32435113_32435114delinsAGCA2740093681WT1c.247_248delinsCT (p.Ala83Leu)
c.232_233delinsCT (p.Ala78Leu)
n.426_427delinsCT
ClinVar
11g.32435114C>ACA10634698WT1c.247G>T (p.Ala83Ser)
c.232G>T (p.Ala78Ser)
n.426G>T
ClinVar dbSNP gnomAD v4
11g.32435114C=CA1962327343WT1c.247G= (p.Ala83=)
c.232G= (p.Ala78=)
n.426G=
11g.32435114C>GCA379966074WT1c.247G>C (p.Ala83Pro)
c.232G>C (p.Ala78Pro)
n.426G>C
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435114C>TCA379966075WT1c.247G>A (p.Ala83Thr)
c.232G>A (p.Ala78Thr)
n.426G>A
ClinVar gnomAD v4
11g.32435115G>ACA473774047WT1c.246C>T (p.Asn82=)
c.231C>T (p.Asn77=)
n.425C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435115G>CCA379966076WT1c.246C>G (p.Asn82Lys)
c.231C>G (p.Asn77Lys)
n.425C>G
ClinVar
11g.32435115G=CA1962327344WT1c.246C= (p.Asn82=)
c.231C= (p.Asn77=)
n.425C=
11g.32435115G>TCA379966077WT1c.246C>A (p.Asn82Lys)
c.231C>A (p.Asn77Lys)
n.425C>A
ClinVar gnomAD v4
11g.32435116T>ACA379966078WT1c.245A>T (p.Asn82Ile)
c.230A>T (p.Asn77Ile)
n.424A>T
11g.32435116T>CCA379966079WT1c.245A>G (p.Asn82Ser)
c.230A>G (p.Asn77Ser)
n.424A>G
11g.32435116T>GCA379966080WT1c.245A>C (p.Asn82Thr)
c.230A>C (p.Asn77Thr)
n.424A>C
dbSNP
11g.32435117T>ACA379966081WT1c.244A>T (p.Asn82Tyr)
c.229A>T (p.Asn77Tyr)
n.423A>T
11g.32435117T>CCA379966082WT1c.244A>G (p.Asn82Asp)
c.229A>G (p.Asn77Asp)
n.423A>G
ClinVar gnomAD v4
11g.32435117T>GCA379966083WT1c.244A>C (p.Asn82His)
c.229A>C (p.Asn77His)
n.423A>C
11g.32435118C>ACA473774054WT1c.243G>T (p.Leu81=)
c.228G>T (p.Leu76=)
n.422G>T
gnomAD v4
11g.32435118C>GCA473774055WT1c.243G>C (p.Leu81=)
c.228G>C (p.Leu76=)
n.422G>C
11g.32435118C>TCA473774056WT1c.243G>A (p.Leu81=)
c.228G>A (p.Leu76=)
n.422G>A
gnomAD v4
11g.32435119A>CCA379966086WT1c.242T>G (p.Leu81Arg)
c.227T>G (p.Leu76Arg)
n.421T>G
ClinVar dbSNP
11g.32435119A>GCA379966085WT1c.242T>C (p.Leu81Pro)
c.227T>C (p.Leu76Pro)
n.421T>C
dbSNP gnomAD v4
11g.32435119A>TCA379966084WT1c.242T>A (p.Leu81Gln)
c.227T>A (p.Leu76Gln)
n.421T>A
gnomAD v4
11g.32435120G>ACA473774057WT1c.241C>T (p.Leu81=)
c.226C>T (p.Leu76=)
n.420C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435120G>CCA064777WT1c.241C>G (p.Leu81Val)
c.226C>G (p.Leu76Val)
n.420C>G
dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435120G=CA1962327345WT1c.241C= (p.Leu81=)
c.226C= (p.Leu76=)
n.420C=
11g.32435120G>TCA379966087WT1c.241C>A (p.Leu81Met)
c.226C>A (p.Leu76Met)
n.420C>A
ClinVar dbSNP gnomAD v4
11g.32435121G>ACA473774063WT1c.240C>T (p.Asp80=)
c.225C>T (p.Asp75=)
n.419C>T
gnomAD v4
11g.32435121G>CCA379966088WT1c.240C>G (p.Asp80Glu)
c.225C>G (p.Asp75Glu)
n.419C>G
ClinVar dbSNP gnomAD v4
11g.32435121G>TCA379966089WT1c.240C>A (p.Asp80Glu)
c.225C>A (p.Asp75Glu)
n.419C>A
gnomAD v4
11g.32435122T>ACA379966090WT1c.239A>T (p.Asp80Val)
c.224A>T (p.Asp75Val)
n.418A>T
11g.32435122T>CCA379966091WT1c.239A>G (p.Asp80Gly)
c.224A>G (p.Asp75Gly)
n.418A>G
ClinVar gnomAD v4
11g.32435122T>GCA379966092WT1c.239A>C (p.Asp80Ala)
c.224A>C (p.Asp75Ala)
n.418A>C
11g.32435123C>ACA379966093WT1c.238G>T (p.Asp80Tyr)
c.223G>T (p.Asp75Tyr)
n.417G>T
gnomAD v4
11g.32435123C>GCA379966094WT1c.238G>C (p.Asp80His)
c.223G>C (p.Asp75His)
n.417G>C
ClinVar
11g.32435123C>TCA379966095WT1c.238G>A (p.Asp80Asn)
c.223G>A (p.Asp75Asn)
n.417G>A
11g.32435125delCA2612989627WT1c.238del (p.Asp80ThrfsTer2)
c.223del (p.Asp75ThrfsTer2)
n.417del
gnomAD v4
11g.32435124C>ACA473774070WT1c.237G>T (p.Arg79=)
c.222G>T (p.Arg74=)
n.416G>T
gnomAD v4
11g.32435124C=CA1962327346WT1c.237G= (p.Arg79=)
c.222G= (p.Arg74=)
n.416G=
11g.32435124C>GCA473774074WT1c.237G>C (p.Arg79=)
c.222G>C (p.Arg74=)
n.416G>C
ClinVar dbSNP gnomAD v4
11g.32435124C>TCA473774072WT1c.237G>A (p.Arg79=)
c.222G>A (p.Arg74=)
n.416G>A
ClinVar gnomAD v4
11g.32435125C>ACA379966096WT1c.236G>T (p.Arg79Leu)
c.221G>T (p.Arg74Leu)
n.415G>T
gnomAD v4
11g.32435125C=CA1962327347WT1c.236G= (p.Arg79=)
c.221G= (p.Arg74=)
n.415G=
11g.32435125C>GCA379966097WT1c.236G>C (p.Arg79Pro)
c.221G>C (p.Arg74Pro)
n.415G>C
gnomAD v4
11g.32435125C>TCA379966098WT1c.236G>A (p.Arg79Gln)
c.221G>A (p.Arg74Gln)
n.415G>A
ClinVar dbSNP gnomAD v4
11g.32435126G>ACA379966099WT1c.235C>T (p.Arg79Trp)
c.220C>T (p.Arg74Trp)
n.414C>T
dbSNP gnomAD v4
11g.32435126G>CCA379966100WT1c.235C>G (p.Arg79Gly)
c.220C>G (p.Arg74Gly)
n.414C>G
11g.32435126G=CA1962327348WT1c.235C= (p.Arg79=)
c.220C= (p.Arg74=)
n.414C=
11g.32435126G>TCA473774078WT1c.235C>A (p.Arg79=)
c.220C>A (p.Arg74=)
n.414C>A
gnomAD v4
11g.32435127C>ACA473774079WT1c.234G>T (p.Val78=)
c.219G>T (p.Val73=)
n.413G>T
gnomAD v4
11g.32435127C>GCA473774082WT1c.234G>C (p.Val78=)
c.219G>C (p.Val73=)
n.413G>C
11g.32435127C>TCA473774084WT1c.234G>A (p.Val78=)
c.219G>A (p.Val73=)
n.413G>A
gnomAD v4
11g.32435128A>CCA379966101WT1c.233T>G (p.Val78Gly)
c.218T>G (p.Val73Gly)
n.412T>G
11g.32435128A>GCA379966103WT1c.233T>C (p.Val78Ala)
c.218T>C (p.Val73Ala)
n.412T>C
gnomAD v4
11g.32435128A>TCA379966102WT1c.233T>A (p.Val78Glu)
c.218T>A (p.Val73Glu)
n.412T>A
11g.32435129C>ACA379966104WT1c.232G>T (p.Val78Leu)
c.217G>T (p.Val73Leu)
n.411G>T
ClinVar gnomAD v4
11g.32435129C=CA1962327349WT1c.232G= (p.Val78=)
c.217G= (p.Val73=)
n.411G=
11g.32435129C>GCA379966105WT1c.232G>C (p.Val78Leu)
c.217G>C (p.Val73Leu)
n.411G>C
gnomAD v4
11g.32435129C>TCA379966106WT1c.232G>A (p.Val78Met)
c.217G>A (p.Val73Met)
n.411G>A
ClinVar dbSNP gnomAD v4
11g.32435130G>ACA473774085WT1c.231C>T (p.Asp77=)
c.216C>T (p.Asp72=)
n.410C>T
ClinVar dbSNP gnomAD v4
11g.32435130G>CCA379966107WT1c.231C>G (p.Asp77Glu)
c.216C>G (p.Asp72Glu)
n.410C>G
11g.32435130G=CA1962327350WT1c.231C= (p.Asp77=)
c.216C= (p.Asp72=)
n.410C=
11g.32435130G>TCA379966108WT1c.231C>A (p.Asp77Glu)
c.216C>A (p.Asp72Glu)
n.410C>A
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435131T>ACA379966111WT1c.230A>T (p.Asp77Val)
c.215A>T (p.Asp72Val)
n.409A>T
ClinVar dbSNP gnomAD v4
11g.32435131T>CCA379966110WT1c.230A>G (p.Asp77Gly)
c.215A>G (p.Asp72Gly)
n.409A>G
gnomAD v4
11g.32435131T>GCA379966109WT1c.230A>C (p.Asp77Ala)
c.215A>C (p.Asp72Ala)
n.409A>C
11g.32435132C>ACA379966112WT1c.229G>T (p.Asp77Tyr)
c.214G>T (p.Asp72Tyr)
n.408G>T
gnomAD v4
11g.32435132C>GCA379966113WT1c.229G>C (p.Asp77His)
c.214G>C (p.Asp72His)
n.408G>C
gnomAD v4
11g.32435132C>TCA379966114WT1c.229G>A (p.Asp77Asn)
c.214G>A (p.Asp72Asn)
n.408G>A
dbSNP gnomAD v4
11g.32435133G>ACA473774094WT1c.228C>T (p.Ser76=)
c.213C>T (p.Ser71=)
n.407C>T
ClinVar dbSNP gnomAD v4
11g.32435133G>CCA473774098WT1c.228C>G (p.Ser76=)
c.213C>G (p.Ser71=)
n.407C>G
ClinVar gnomAD v4
11g.32435133G>TCA473774100WT1c.228C>A (p.Ser76=)
c.213C>A (p.Ser71=)
n.407C>A
gnomAD v4
11g.32435134G>ACA379966115WT1c.227C>T (p.Ser76Phe)
c.212C>T (p.Ser71Phe)
n.406C>T
gnomAD v4
11g.32435134G>CCA379966116WT1c.227C>G (p.Ser76Cys)
c.212C>G (p.Ser71Cys)
n.406C>G
11g.32435134G>TCA379966117WT1c.227C>A (p.Ser76Tyr)
c.212C>A (p.Ser71Tyr)
n.406C>A
gnomAD v4
11g.32435135A>CCA379966120WT1c.226T>G (p.Ser76Ala)
c.211T>G (p.Ser71Ala)
n.405T>G
11g.32435135A>GCA379966118WT1c.226T>C (p.Ser76Pro)
c.211T>C (p.Ser71Pro)
n.405T>C
dbSNP
11g.32435135A>TCA379966119WT1c.226T>A (p.Ser76Thr)
c.211T>A (p.Ser71Thr)
n.405T>A
dbSNP gnomAD v4
11g.32435136delCA2740093682WT1c.225del (p.Ser76ProfsTer6)
c.210del (p.Ser71ProfsTer6)
n.404del
ClinVar
11g.32435136G>ACA473774105WT1c.225C>T (p.Gly75=)
c.210C>T (p.Gly70=)
n.404C>T
ClinVar dbSNP
11g.32435136G>CCA473774106WT1c.225C>G (p.Gly75=)
c.210C>G (p.Gly70=)
n.404C>G
ClinVar dbSNP
11g.32435136G=CA1962327351WT1c.225C= (p.Gly75=)
c.210C= (p.Gly70=)
n.404C=
11g.32435136G>TCA473774108WT1c.225C>A (p.Gly75=)
c.210C>A (p.Gly70=)
n.404C>A
ClinVar dbSNP gnomAD v4
11g.32435137C>ACA379966121WT1c.224G>T (p.Gly75Val)
c.209G>T (p.Gly70Val)
n.403G>T
11g.32435137C=CA1962327352WT1c.224G= (p.Gly75=)
c.209G= (p.Gly70=)
n.403G=
11g.32435137C>GCA379966122WT1c.224G>C (p.Gly75Ala)
c.209G>C (p.Gly70Ala)
n.403G>C
COSMIC COSMIC
11g.32435137C>TCA379966123WT1c.224G>A (p.Gly75Asp)
c.209G>A (p.Gly70Asp)
n.403G>A
dbSNP gnomAD v2 gnomAD v4
11g.32435138C>ACA379966124WT1c.223G>T (p.Gly75Cys)
c.208G>T (p.Gly70Cys)
n.402G>T
dbSNP gnomAD v4
11g.32435138C=CA1962327353WT1c.223G= (p.Gly75=)
c.208G= (p.Gly70=)
n.402G=
11g.32435138C>GCA379966125WT1c.223G>C (p.Gly75Arg)
c.208G>C (p.Gly70Arg)
n.402G>C
11g.32435138C>TCA064759WT1c.223G>A (p.Gly75Ser)
c.208G>A (p.Gly70Ser)
n.402G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435139C>ACA379966126WT1c.222G>T (p.Met74Ile)
c.207G>T (p.Met69Ile)
n.401G>T
dbSNP
11g.32435139C>GCA379966127WT1c.222G>C (p.Met74Ile)
c.207G>C (p.Met69Ile)
n.401G>C
11g.32435139C>TCA379966128WT1c.222G>A (p.Met74Ile)
c.207G>A (p.Met69Ile)
n.401G>A
gnomAD v4
11g.32435140A>CCA379966129WT1c.221T>G (p.Met74Arg)
c.206T>G (p.Met69Arg)
n.400T>G
dbSNP
11g.32435140A>GCA379966130WT1c.221T>C (p.Met74Thr)
c.206T>C (p.Met69Thr)
n.400T>C
gnomAD v4
11g.32435140A>TCA379966131WT1c.221T>A (p.Met74Lys)
c.206T>A (p.Met69Lys)
n.400T>A
dbSNP
11g.32435141T>ACA379966134WT1c.220A>T (p.Met74Leu)
c.205A>T (p.Met69Leu)
n.399A>T
gnomAD v4
11g.32435141T>CCA379966132WT1c.220A>G (p.Met74Val)
c.205A>G (p.Met69Val)
n.399A>G
ClinVar
11g.32435141T>GCA379966133WT1c.220A>C (p.Met74Leu)
c.205A>C (p.Met69Leu)
n.399A>C
11g.32435142T>ACA379966135WT1c.219A>T (p.Gln73His)
c.204A>T (p.Gln68His)
n.398A>T
11g.32435142T>CCA473774117WT1c.219A>G (p.Gln73=)
c.204A>G (p.Gln68=)
n.398A>G
gnomAD v4
11g.32435142T>GCA379966136WT1c.219A>C (p.Gln73His)
c.204A>C (p.Gln68His)
n.398A>C
11g.32435143T>ACA219511297WT1c.218A>T (p.Gln73Leu)
c.203A>T (p.Gln68Leu)
n.397A>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435143T>CCA379966137WT1c.218A>G (p.Gln73Arg)
c.203A>G (p.Gln68Arg)
n.397A>G
11g.32435143T>GCA379966138WT1c.218A>C (p.Gln73Pro)
c.203A>C (p.Gln68Pro)
n.397A>C
11g.32435143T=CA1962327354WT1c.218A= (p.Gln73=)
c.203A= (p.Gln68=)
n.397A=
11g.32435144G>ACA379966139WT1c.217C>T (p.Gln73Ter)
c.202C>T (p.Gln68Ter)
n.396C>T
gnomAD v4
11g.32435144G>CCA379966140WT1c.217C>G (p.Gln73Glu)
c.202C>G (p.Gln68Glu)
n.396C>G
11g.32435144G>TCA379966141WT1c.217C>A (p.Gln73Lys)
c.202C>A (p.Gln68Lys)
n.396C>A
gnomAD v4
11g.32435145C>ACA064754WT1c.216G>T (p.Gln72His)
c.201G>T (p.Gln67His)
n.395G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.32435145C=CA1962327355WT1c.216G= (p.Gln72=)
c.201G= (p.Gln67=)
n.395G=
11g.32435145C>GCA379966142WT1c.216G>C (p.Gln72His)
c.201G>C (p.Gln67His)
n.395G>C
ClinVar dbSNP gnomAD v4
11g.32435145C>TCA473774125WT1c.216G>A (p.Gln72=)
c.201G>A (p.Gln67=)
n.395G>A
ClinVar gnomAD v4
11g.32435146T>ACA379966143WT1c.215A>T (p.Gln72Leu)
c.200A>T (p.Gln67Leu)
n.394A>T
ClinVar dbSNP gnomAD v4
11g.32435146T>CCA379966144WT1c.215A>G (p.Gln72Arg)
c.200A>G (p.Gln67Arg)
n.394A>G
gnomAD v4
11g.32435146T>GCA379966145WT1c.215A>C (p.Gln72Pro)
c.200A>C (p.Gln67Pro)
n.394A>C
11g.32435147G>ACA379966148WT1c.214C>T (p.Gln72Ter)
c.199C>T (p.Gln67Ter)
n.393C>T
gnomAD v4
11g.32435147G>CCA379966146WT1c.214C>G (p.Gln72Glu)
c.199C>G (p.Gln67Glu)
n.393C>G
11g.32435147G>TCA379966147WT1c.214C>A (p.Gln72Lys)
c.199C>A (p.Gln67Lys)
n.393C>A
gnomAD v4
11g.32435148C>ACA064733WT1c.213G>T (p.Pro71=)
c.198G>T (p.Pro66=)
n.392G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435148C=CA1962327356WT1c.213G= (p.Pro71=)
c.198G= (p.Pro66=)
n.392G=
11g.32435148C>GCA473774132WT1c.213G>C (p.Pro71=)
c.198G>C (p.Pro66=)
n.392G>C
gnomAD v4
11g.32435148C>TCA473774133WT1c.213G>A (p.Pro71=)
c.198G>A (p.Pro66=)
n.392G>A
dbSNP gnomAD v4
11g.32435149G>ACA379966149WT1c.212C>T (p.Pro71Leu)
c.197C>T (p.Pro66Leu)
n.391C>T
gnomAD v4
11g.32435149G>CCA379966150WT1c.212C>G (p.Pro71Arg)
c.197C>G (p.Pro66Arg)
n.391C>G
11g.32435149G>TCA379966151WT1c.212C>A (p.Pro71Gln)
c.197C>A (p.Pro66Gln)
n.391C>A
gnomAD v4
11g.32435150G>ACA379966152WT1c.211C>T (p.Pro71Ser)
c.196C>T (p.Pro66Ser)
n.390C>T
ClinVar dbSNP gnomAD v4
11g.32435150G>CCA379966153WT1c.211C>G (p.Pro71Ala)
c.196C>G (p.Pro66Ala)
n.390C>G
gnomAD v4
11g.32435150G=CA1962327357WT1c.211C= (p.Pro71=)
c.196C= (p.Pro66=)
n.390C=
11g.32435150G>TCA379966154WT1c.211C>A (p.Pro71Thr)
c.196C>A (p.Pro66Thr)
n.390C>A
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435151C>ACA064727WT1c.210G>T (p.Glu70Asp)
c.195G>T (p.Glu65Asp)
n.389G>T
dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435151C=CA1962327358WT1c.210G= (p.Glu70=)
c.195G= (p.Glu65=)
n.389G=
11g.32435151C>GCA379966155WT1c.210G>C (p.Glu70Asp)
c.195G>C (p.Glu65Asp)
n.389G>C
ClinVar dbSNP
11g.32435151C>TCA473774138WT1c.210G>A (p.Glu70=)
c.195G>A (p.Glu65=)
n.389G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435152T>ACA379966156WT1c.209A>T (p.Glu70Val)
c.194A>T (p.Glu65Val)
n.388A>T
11g.32435152T>CCA379966157WT1c.209A>G (p.Glu70Gly)
c.194A>G (p.Glu65Gly)
n.388A>G
dbSNP gnomAD v4
11g.32435152T>GCA379966158WT1c.209A>C (p.Glu70Ala)
c.194A>C (p.Glu65Ala)
n.388A>C
11g.32435153C>ACA379966159WT1c.208G>T (p.Glu70Ter)
c.193G>T (p.Glu65Ter)
n.387G>T
gnomAD v4
11g.32435153C>GCA379966161WT1c.208G>C (p.Glu70Gln)
c.193G>C (p.Glu65Gln)
n.387G>C
gnomAD v4
11g.32435153C>TCA379966160WT1c.208G>A (p.Glu70Lys)
c.193G>A (p.Glu65Lys)
n.387G>A
dbSNP
11g.32435154A>CCA473774143WT1c.207T>G (p.Ser69=)
c.192T>G (p.Ser64=)
n.386T>G
11g.32435154A>GCA473774146WT1c.207T>C (p.Ser69=)
c.192T>C (p.Ser64=)
n.386T>C
gnomAD v4
11g.32435154A>TCA473774150WT1c.207T>A (p.Ser69=)
c.192T>A (p.Ser64=)
n.386T>A
11g.32435155G>ACA379966162WT1c.206C>T (p.Ser69Phe)
c.191C>T (p.Ser64Phe)
n.385C>T
11g.32435155G>CCA379966164WT1c.206C>G (p.Ser69Cys)
c.191C>G (p.Ser64Cys)
n.385C>G
11g.32435155G>TCA379966163WT1c.206C>A (p.Ser69Tyr)
c.191C>A (p.Ser64Tyr)
n.385C>A
11g.32435156A=CA1962327359WT1c.205T= (p.Ser69=)
c.190T= (p.Ser64=)
n.384T=
11g.32435156A>CCA379966165WT1c.205T>G (p.Ser69Ala)
c.190T>G (p.Ser64Ala)
n.384T>G
dbSNP
11g.32435156A>GCA379966166WT1c.205T>C (p.Ser69Pro)
c.190T>C (p.Ser64Pro)
n.384T>C
gnomAD v4
11g.32435156A>TCA379966167WT1c.205T>A (p.Ser69Thr)
c.190T>A (p.Ser64Thr)
n.384T>A
ClinVar dbSNP gnomAD v4
11g.32435157C>ACA473774152WT1c.204G>T (p.Gly68=)
c.189G>T (p.Gly63=)
n.383G>T
gnomAD v4
11g.32435157C=CA1962327360WT1c.204G= (p.Gly68=)
c.189G= (p.Gly63=)
n.383G=
11g.32435157C>GCA473774153WT1c.204G>C (p.Gly68=)
c.189G>C (p.Gly63=)
n.383G>C
gnomAD v4
11g.32435157C>TCA473774155WT1c.204G>A (p.Gly68=)
c.189G>A (p.Gly63=)
n.383G>A
ClinVar dbSNP gnomAD v4
11g.32435158C>ACA379966168WT1c.203G>T (p.Gly68Val)
c.188G>T (p.Gly63Val)
n.382G>T
gnomAD v4
11g.32435158C=CA1962327361WT1c.203G= (p.Gly68=)
c.188G= (p.Gly63=)
n.382G=
11g.32435158C>GCA379966169WT1c.203G>C (p.Gly68Ala)
c.188G>C (p.Gly63Ala)
n.382G>C
gnomAD v4
11g.32435158C>TCA379966170WT1c.203G>A (p.Gly68Glu)
c.188G>A (p.Gly63Glu)
n.382G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435159C>ACA379966171WT1c.202G>T (p.Gly68Trp)
c.187G>T (p.Gly63Trp)
n.381G>T
dbSNP gnomAD v4
11g.32435159C=CA1962327362WT1c.202G= (p.Gly68=)
c.187G= (p.Gly63=)
n.381G=
11g.32435159C>GCA379966172WT1c.202G>C (p.Gly68Arg)
c.187G>C (p.Gly63Arg)
n.381G>C
ClinVar dbSNP gnomAD v4
11g.32435159C>TCA379966173WT1c.202G>A (p.Gly68Arg)
c.187G>A (p.Gly63Arg)
n.381G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435160G>ACA473774158WT1c.201C>T (p.Ser67=)
c.186C>T (p.Ser62=)
n.380C>T
ClinVar dbSNP gnomAD v4
11g.32435160G>CCA064720WT1c.201C>G (p.Ser67=)
c.186C>G (p.Ser62=)
n.380C>G
dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435160G=CA1962327363WT1c.201C= (p.Ser67=)
c.186C= (p.Ser62=)
n.380C=
11g.32435160G>TCA473774161WT1c.201C>A (p.Ser67=)
c.186C>A (p.Ser62=)
n.380C>A
gnomAD v4
11g.32435161G>ACA379966174WT1c.200C>T (p.Ser67Phe)
c.185C>T (p.Ser62Phe)
n.379C>T
ClinVar dbSNP gnomAD v4
11g.32435161G>CCA379966175WT1c.200C>G (p.Ser67Cys)
c.185C>G (p.Ser62Cys)
n.379C>G
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435161G=CA1962327364WT1c.200C= (p.Ser67=)
c.185C= (p.Ser62=)
n.379C=
11g.32435161G>TCA379966176WT1c.200C>A (p.Ser67Tyr)
c.185C>A (p.Ser62Tyr)
n.379C>A
dbSNP gnomAD v4
11g.32435162A>CCA379966177WT1c.199T>G (p.Ser67Ala)
c.184T>G (p.Ser62Ala)
n.378T>G
11g.32435162A>GCA379966179WT1c.199T>C (p.Ser67Pro)
c.184T>C (p.Ser62Pro)
n.378T>C
dbSNP gnomAD v4
11g.32435162A>TCA379966178WT1c.199T>A (p.Ser67Thr)
c.184T>A (p.Ser62Thr)
n.378T>A
11g.32435163delCA2612989662WT1c.198del (p.Ser67ProfsTer15)
c.183del (p.Ser62ProfsTer15)
n.377del
gnomAD v4
11g.32435163C>ACA219511329WT1c.198G>T (p.Ala66=)
c.183G>T (p.Ala61=)
n.377G>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435163C=CA1962327365WT1c.198G= (p.Ala66=)
c.183G= (p.Ala61=)
n.377G=
11g.32435163C>GCA473774168WT1c.198G>C (p.Ala66=)
c.183G>C (p.Ala61=)
n.377G>C
11g.32435163C>TCA473774169WT1c.198G>A (p.Ala66=)
c.183G>A (p.Ala61=)
n.377G>A
ClinVar dbSNP gnomAD v4 COSMIC
11g.32435164G>ACA379966180WT1c.197C>T (p.Ala66Val)
c.182C>T (p.Ala61Val)
n.376C>T
ClinVar dbSNP gnomAD v4 COSMIC
11g.32435164G>CCA379966181WT1c.197C>G (p.Ala66Gly)
c.182C>G (p.Ala61Gly)
n.376C>G
dbSNP gnomAD v3 gnomAD v4
11g.32435164G=CA1962327366WT1c.197C= (p.Ala66=)
c.182C= (p.Ala61=)
n.376C=
11g.32435164G>TCA379966182WT1c.197C>A (p.Ala66Glu)
c.182C>A (p.Ala61Glu)
n.376C>A
ClinVar dbSNP gnomAD v4
11g.32435165C>ACA379966183WT1c.196G>T (p.Ala66Ser)
c.181G>T (p.Ala61Ser)
n.375G>T
11g.32435165C=CA1962327367WT1c.196G= (p.Ala66=)
c.181G= (p.Ala61=)
n.375G=
11g.32435165C>GCA379966184WT1c.196G>C (p.Ala66Pro)
c.181G>C (p.Ala61Pro)
n.375G>C
11g.32435165C>TCA379966185WT1c.196G>A (p.Ala66Thr)
c.181G>A (p.Ala61Thr)
n.375G>A
ClinVar dbSNP gnomAD v4
11g.32435168delCA2612989664WT1c.196del (p.Ala66ArgfsTer16)
c.181del (p.Ala61ArgfsTer16)
n.375del
ClinVar gnomAD v4
11g.32435166C>ACA473774171WT1c.195G>T (p.Gly65=)
c.180G>T (p.Gly60=)
n.374G>T
gnomAD v4
11g.32435166C=CA1962327368WT1c.195G= (p.Gly65=)
c.180G= (p.Gly60=)
n.374G=
11g.32435166C>GCA473774173WT1c.195G>C (p.Gly65=)
c.180G>C (p.Gly60=)
n.374G>C
11g.32435166C>TCA473774172WT1c.195G>A (p.Gly65=)
c.180G>A (p.Gly60=)
n.374G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435167C>ACA379966186WT1c.194G>T (p.Gly65Val)
c.179G>T (p.Gly60Val)
n.373G>T
gnomAD v4
11g.32435167C=CA1962327369WT1c.194G= (p.Gly65=)
c.179G= (p.Gly60=)
n.373G=
11g.32435167C>GCA379966187WT1c.194G>C (p.Gly65Ala)
c.179G>C (p.Gly60Ala)
n.373G>C
11g.32435167C>TCA379966188WT1c.194G>A (p.Gly65Glu)
c.179G>A (p.Gly60Glu)
n.373G>A
ClinVar dbSNP gnomAD v4
11g.32435168C>ACA379966190WT1c.193G>T (p.Gly65Trp)
c.178G>T (p.Gly60Trp)
n.372G>T
ClinVar dbSNP gnomAD v4
11g.32435168C=CA1962327370WT1c.193G= (p.Gly65=)
c.178G= (p.Gly60=)
n.372G=
11g.32435168C>GCA379966189WT1c.193G>C (p.Gly65Arg)
c.178G>C (p.Gly60Arg)
n.372G>C
11g.32435168C>TCA064714WT1c.193G>A (p.Gly65Arg)
c.178G>A (p.Gly60Arg)
n.372G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435169G>ACA473774180WT1c.192C>T (p.Arg64=)
c.177C>T (p.Arg59=)
n.371C>T
gnomAD v4
11g.32435169G>CCA473774181WT1c.192C>G (p.Arg64=)
c.177C>G (p.Arg59=)
n.371C>G
dbSNP
11g.32435169G=CA1962327371WT1c.192C= (p.Arg64=)
c.177C= (p.Arg59=)
n.371C=
11g.32435169G>TCA473774182WT1c.192C>A (p.Arg64=)
c.177C>A (p.Arg59=)
n.371C>A
dbSNP gnomAD v4
11g.32435170C>ACA379966191WT1c.191G>T (p.Arg64Leu)
c.176G>T (p.Arg59Leu)
n.370G>T
ClinVar gnomAD v4
11g.32435170C=CA1962327372WT1c.191G= (p.Arg64=)
c.176G= (p.Arg59=)
n.370G=
11g.32435170C>GCA379966192WT1c.191G>C (p.Arg64Pro)
c.176G>C (p.Arg59Pro)
n.370G>C
11g.32435170C>TCA379966193WT1c.191G>A (p.Arg64His)
c.176G>A (p.Arg59His)
n.370G>A
ClinVar dbSNP gnomAD v4
11g.32435171G>ACA379966194WT1c.190C>T (p.Arg64Cys)
c.175C>T (p.Arg59Cys)
n.369C>T
gnomAD v4
11g.32435171G>CCA379966195WT1c.190C>G (p.Arg64Gly)
c.175C>G (p.Arg59Gly)
n.369C>G
dbSNP gnomAD v2 gnomAD v4
11g.32435171G=CA1962327373WT1c.190C= (p.Arg64=)
c.175C= (p.Arg59=)
n.369C=
11g.32435171G>TCA379966196WT1c.190C>A (p.Arg64Ser)
c.175C>A (p.Arg59Ser)
n.369C>A
gnomAD v4
11g.32435172G>ACA473774184WT1c.189C>T (p.Ser63=)
c.174C>T (p.Ser58=)
n.368C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435172G>CCA379966197WT1c.189C>G (p.Ser63Arg)
c.174C>G (p.Ser58Arg)
n.368C>G
gnomAD v4
11g.32435172G=CA1962327374WT1c.189C= (p.Ser63=)
c.174C= (p.Ser58=)
n.368C=
11g.32435172G>TCA379966198WT1c.189C>A (p.Ser63Arg)
c.174C>A (p.Ser58Arg)
n.368C>A
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435173C>ACA379966199WT1c.188G>T (p.Ser63Ile)
c.173G>T (p.Ser58Ile)
n.367G>T
gnomAD v4
11g.32435173C>GCA379966200WT1c.188G>C (p.Ser63Thr)
c.173G>C (p.Ser58Thr)
n.367G>C
11g.32435173C>TCA379966201WT1c.188G>A (p.Ser63Asn)
c.173G>A (p.Ser58Asn)
n.367G>A
gnomAD v4
11g.32435174T>ACA379966204WT1c.187A>T (p.Ser63Cys)
c.172A>T (p.Ser58Cys)
n.366A>T
11g.32435174T>CCA379966203WT1c.187A>G (p.Ser63Gly)
c.172A>G (p.Ser58Gly)
n.366A>G
dbSNP gnomAD v3 gnomAD v4
11g.32435174T>GCA379966202WT1c.187A>C (p.Ser63Arg)
c.172A>C (p.Ser58Arg)
n.366A>C
11g.32435175C>ACA379966205WT1c.186G>T (p.Arg62Ser)
c.171G>T (p.Arg57Ser)
n.365G>T
gnomAD v4
11g.32435175C=CA1962327375WT1c.186G= (p.Arg62=)
c.171G= (p.Arg57=)
n.365G=
11g.32435175C>GCA379966206WT1c.186G>C (p.Arg62Ser)
c.171G>C (p.Arg57Ser)
n.365G>C
11g.32435175C>TCA473774185WT1c.186G>A (p.Arg62=)
c.171G>A (p.Arg57=)
n.365G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435176C>ACA379966207WT1c.185G>T (p.Arg62Met)
c.170G>T (p.Arg57Met)
n.364G>T
gnomAD v4
11g.32435176C=CA1962327376WT1c.185G= (p.Arg62=)
c.170G= (p.Arg57=)
n.364G=
11g.32435176C>GCA379966208WT1c.185G>C (p.Arg62Thr)
c.170G>C (p.Arg57Thr)
n.364G>C
11g.32435176C>TCA379966209WT1c.185G>A (p.Arg62Lys)
c.170G>A (p.Arg57Lys)
n.364G>A
ClinVar dbSNP gnomAD v4
11g.32435177delCA2612989671WT1c.184del (p.Arg62GlyfsTer20)
c.169del (p.Arg57GlyfsTer20)
n.363del
gnomAD v4
11g.32435177T>ACA379966210WT1c.184A>T (p.Arg62Trp)
c.169A>T (p.Arg57Trp)
n.363A>T
gnomAD v4
11g.32435177T>CCA379966211WT1c.184A>G (p.Arg62Gly)
c.169A>G (p.Arg57Gly)
n.363A>G
dbSNP gnomAD v4
11g.32435177T>GCA473774188WT1c.184A>C (p.Arg62=)
c.169A>C (p.Arg57=)
n.363A>C
gnomAD v4

Number of alleles fetched