Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25012021_25015415delCA915950806ARXc.196+129_1073+903del
ClinVar
Xg.25013627_25013674delCA2693353732ARXc.323_370del (p.Ala108_Gly123del)
gnomAD v4
Xg.25013650_25013691dupCA16621352ARXc.304_345dup (p.Ala115_Thr116insAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAla)
ClinVar dbSNP
Xg.25013653_25013674delinsGGCCGCTGCCGCCGCCGCCGCCCA2420209372ARXc.321_342delinsGGCGGCGGCGGCGGCAGCGGCC (p.Ala107=)
Xg.25013653_25013680delinsGGCCGCTGCCGCCGCCGCCGCCGCCGCCCA2420209375ARXc.315_342delinsGGCGGCGGCGGCGGCGGCGGCAGCGGCC (p.Ala105=)
Xg.25013653_25013686delinsGGCCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCCA2420209378ARXc.309_342delinsGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCC (p.Ala103=)
Xg.25013659_25013667delCA2420209381ARXc.333_341del (p.Ala112_Ala114del)
dbSNP
Xg.25013659_25013670delCA1131757349ARXc.330_341del (p.Ala111_Ala114del)
dbSNP gnomAD v3 gnomAD v4
Xg.25013659_25013676delCA2573158503ARXc.324_341del (p.Ala109_Ala114del)
ClinVar dbSNP
Xg.25013659_25013679delCA658799628ARXc.321_341del (p.Ala108_Ala114del)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25013659_25013685delCA2420209379ARXc.315_341del (p.Ala106_Ala114del)
dbSNP
Xg.25013665_25013697dupCA891843652ARXc.309_341dup (p.Ala114_Ala115insAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAla)
ClinVar dbSNP
Xg.25013665_25013697delCA874147898ARXc.309_341del (p.Ala104_Ala114del)
dbSNP gnomAD v3 gnomAD v4
Xg.25013659_25013677delinsTGCCGCCGCCGCCGCCGCCCA2420209385ARXc.318_336delinsGGCGGCGGCGGCGGCGGCA (p.Ala106=)
Xg.25013689_25013691dupCA171154ARXc.333_335dup (p.Ala112_Ala113insAla)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013686_25013691dupCA16621353ARXc.330_335dup (p.Ala112_Ala113insAlaAla)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013683_25013691dupCA241827ARXc.327_335dup (p.Ala112_Ala113insAlaAlaAla)
ClinVar dbSNP gnomAD v4
Xg.25013680_25013691dupCA920402032ARXc.324_335dup (p.Ala112_Ala113insAlaAlaAlaAla)
dbSNP gnomAD v3 gnomAD v4
Xg.25013677_25013691dupCA2580616915ARXc.321_335dup (p.Ala112_Ala113insAlaAlaAlaAlaAla)
ClinVar dbSNP
Xg.25013674_25013691dupCA913187407ARXc.318_335dup (p.Ala112_Ala113insAlaAlaAlaAlaAlaAla)
Xg.25013671_25013691dupCA213330ARXc.315_335dup (p.Ala112_Ala113insAlaAlaAlaAlaAlaAlaAla)
ClinVar dbSNP
Xg.25013668_25013691dupCA213320ARXc.312_335dup (p.Ala112_Ala113insAlaAlaAlaAlaAlaAlaAlaAla)
ClinVar dbSNP
Xg.25013689_25013691delCA16616470ARXc.333_335del (p.Ala112del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013686_25013691delCA171152ARXc.330_335del (p.Ala111_Ala112del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013683_25013691delCA641364635ARXc.327_335del (p.Ala110_Ala112del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013680_25013691delCA241825ARXc.324_335del (p.Ala109_Ala112del)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25013677_25013691delCA874147966ARXc.321_335del (p.Ala108_Ala112del)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25013674_25013691delCA658656857ARXc.318_335del (p.Ala107_Ala112del)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25013671_25013691delCA2580616914ARXc.315_335del (p.Ala106_Ala112del)
ClinVar dbSNP gnomAD v4
Xg.25013668_25013691delCA2569327553ARXc.312_335del (p.Ala105_Ala112del)
Xg.25013666G>ACA412613400ARXc.329C>T (p.Ala110Val)
gnomAD v4
Xg.25013666G>CCA412613401ARXc.329C>G (p.Ala110Gly)
Xg.25013666G>TCA412613402ARXc.329C>A (p.Ala110Glu)
gnomAD v4
Xg.25013667C>ACA412613403ARXc.328G>T (p.Ala110Ser)
Xg.25013667C>GCA412613404ARXc.328G>C (p.Ala110Pro)
Xg.25013667C>TCA412613405ARXc.328G>A (p.Ala110Thr)
gnomAD v4
Xg.25013668C>ACA515948033ARXc.327G>T (p.Ala109=)
gnomAD v4
Xg.25013668C=CA2420209390ARXc.327G= (p.Ala109=)
Xg.25013668C>GCA515948034ARXc.327G>C (p.Ala109=)
Xg.25013668C>TCA515948035ARXc.327G>A (p.Ala109=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013669G>ACA412613406ARXc.326C>T (p.Ala109Val)
gnomAD v4
Xg.25013669G>CCA412613407ARXc.326C>G (p.Ala109Gly)
Xg.25013669G>TCA412613408ARXc.326C>A (p.Ala109Glu)
gnomAD v4
Xg.25013674_25013697dupCA16621354ARXc.303_326dup (p.Ala109_Ala110insAlaAlaAlaAlaAlaAlaAlaAla)
ClinVar dbSNP
Xg.25013670C>ACA412613409ARXc.325G>T (p.Ala109Ser)
Xg.25013670C>GCA412613411ARXc.325G>C (p.Ala109Pro)
Xg.25013670C>TCA412613410ARXc.325G>A (p.Ala109Thr)
gnomAD v4
Xg.25013671C>ACA515948038ARXc.324G>T (p.Ala108=)
gnomAD v4
Xg.25013671C=CA2420209391ARXc.324G= (p.Ala108=)
Xg.25013671C>GCA515948041ARXc.324G>C (p.Ala108=)

Number of alleles fetched