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.25013631_25013664delCA213236ARXc.335_368del (p.Ala112GlyfsTer?)
ClinVar dbSNP
Xg.25013650_25013691dupCA16621352ARXc.304_345dup (p.Ala115_Thr116insAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAla)
ClinVar dbSNP
Xg.25013653_25013665delinsGGCCGCTGCCGCCCA2420209374ARXc.330_342delinsGGCGGCAGCGGCC (p.Ala110=)
Xg.25013653_25013674delinsGGCCGCTGCCGCCGCCGCCGCCCA2420209372ARXc.321_342delinsGGCGGCGGCGGCGGCAGCGGCC (p.Ala107=)
Xg.25013653_25013680delinsGGCCGCTGCCGCCGCCGCCGCCGCCGCCCA2420209375ARXc.315_342delinsGGCGGCGGCGGCGGCGGCGGCAGCGGCC (p.Ala105=)
Xg.25013653_25013686delinsGGCCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCCA2420209378ARXc.309_342delinsGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCC (p.Ala103=)
Xg.25013659_25013664dupCA2693353733ARXc.336_341dup (p.Ala114_Ala115insAlaAla)
gnomAD v4
Xg.25013659_25013664delCA874147897ARXc.336_341del (p.Ala113_Ala114del)
dbSNP
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)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013686_25013691dupCA16621353ARXc.330_335dup (p.Ala112_Ala113insAlaAla)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013683_25013691dupCA241827ARXc.327_335dup (p.Ala112_Ala113insAlaAlaAla)
dbSNP gnomAD v4
Xg.25013680_25013691dupCA920402032ARXc.324_335dup (p.Ala112_Ala113insAlaAlaAlaAla)
dbSNP gnomAD v3 gnomAD v4
Xg.25013677_25013691dupCA2580616915ARXc.321_335dup (p.Ala112_Ala113insAlaAlaAlaAlaAla)
dbSNP
Xg.25013674_25013691dupCA913187407ARXc.318_335dup (p.Ala112_Ala113insAlaAlaAlaAlaAlaAla)
Xg.25013671_25013691dupCA213330ARXc.315_335dup (p.Ala112_Ala113insAlaAlaAlaAlaAlaAlaAla)
dbSNP
Xg.25013668_25013691dupCA213320ARXc.312_335dup (p.Ala112_Ala113insAlaAlaAlaAlaAlaAlaAlaAla)
dbSNP
Xg.25013689_25013691delCA16616470ARXc.333_335del (p.Ala112del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013686_25013691delCA171152ARXc.330_335del (p.Ala111_Ala112del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013683_25013691delCA641364635ARXc.327_335del (p.Ala110_Ala112del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013680_25013691delCA241825ARXc.324_335del (p.Ala109_Ala112del)
dbSNP gnomAD v3 gnomAD v4
Xg.25013677_25013691delCA874147966ARXc.321_335del (p.Ala108_Ala112del)
dbSNP gnomAD v3 gnomAD v4
Xg.25013674_25013691delCA658656857ARXc.318_335del (p.Ala107_Ala112del)
dbSNP gnomAD v3 gnomAD v4
Xg.25013671_25013691delCA2580616914ARXc.315_335del (p.Ala106_Ala112del)
dbSNP gnomAD v4
Xg.25013668_25013691delCA2569327553ARXc.312_335del (p.Ala105_Ala112del)
Xg.25013663G>ACA412613394ARXc.332C>T (p.Ala111Val)
gnomAD v4
Xg.25013663G>CCA412613396ARXc.332C>G (p.Ala111Gly)
gnomAD v4
Xg.25013663G>TCA412613395ARXc.332C>A (p.Ala111Glu)
Xg.25013664_25013665insTGCCA2516781180ARXc.332_333insAGC (p.Ala111_Ala112insAla)
Xg.25013664C>ACA412613397ARXc.331G>T (p.Ala111Ser)
gnomAD v4
Xg.25013664C>GCA412613398ARXc.331G>C (p.Ala111Pro)
Xg.25013664C>TCA412613399ARXc.331G>A (p.Ala111Thr)
gnomAD v4
Xg.25013665C>ACA515948022ARXc.330G>T (p.Ala110=)
Xg.25013665C=CA2420209389ARXc.330G= (p.Ala110=)
Xg.25013665C>GCA515948024ARXc.330G>C (p.Ala110=)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25013665C>TCA515948026ARXc.330G>A (p.Ala110=)
dbSNP gnomAD v4
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)

Number of alleles fetched