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.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
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=

Number of alleles fetched