Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.51141026_51141104delCA2695223381SALL1c.1119_1197del (p.Ser374ArgfsTer17)
c.828_906del (p.Ser277ArgfsTer17)
c.77-3551_77-3473del (n.77-3551_77-3473del)
16g.51141078T>ACA395889350SALL1c.1144A>T (p.Ser382Cys)
c.853A>T (p.Ser285Cys)
c.77-3526A>T (n.77-3526A>T)
16g.51141078T>CCA241494SALL1c.1144A>G (p.Ser382Gly)
c.853A>G (p.Ser285Gly)
c.77-3526A>G (n.77-3526A>G)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.51141078T>GCA395889352SALL1c.1144A>C (p.Ser382Arg)
c.853A>C (p.Ser285Arg)
c.77-3526A>C (n.77-3526A>C)
16g.51141078T=CA2222021331SALL1c.1144A= (p.Ser382=)
c.853A= (p.Ser285=)
c.77-3526A= (n.77-3526A=)
16g.51141079G>ACA8053332SALL1c.1143C>T (p.Ser381=)
c.852C>T (p.Ser284=)
c.77-3527C>T (n.77-3527C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141079G>CCA395889357SALL1c.1143C>G (p.Ser381Arg)
c.852C>G (p.Ser284Arg)
c.77-3527C>G (n.77-3527C>G)
 dbSNP gnomAD v3 gnomAD v4
16g.51141079G=CA2222021337SALL1c.1143C= (p.Ser381=)
c.852C= (p.Ser284=)
c.77-3527C= (n.77-3527C=)
16g.51141079G>TCA395889359SALL1c.1143C>A (p.Ser381Arg)
c.852C>A (p.Ser284Arg)
c.77-3527C>A (n.77-3527C>A)
16g.51141080C>ACA395889361SALL1c.1142G>T (p.Ser381Ile)
c.851G>T (p.Ser284Ile)
c.77-3528G>T (n.77-3528G>T)
16g.51141080C=CA2222021341SALL1c.1142G= (p.Ser381=)
c.851G= (p.Ser284=)
c.77-3528G= (n.77-3528G=)
16g.51141080C>GCA395889365SALL1c.1142G>C (p.Ser381Thr)
c.851G>C (p.Ser284Thr)
c.77-3528G>C (n.77-3528G>C)
16g.51141080C>TCA395889362SALL1c.1142G>A (p.Ser381Asn)
c.851G>A (p.Ser284Asn)
c.77-3528G>A (n.77-3528G>A)
 dbSNP gnomAD v2 gnomAD v4
16g.51141081T>ACA395889368SALL1c.1141A>T (p.Ser381Cys)
c.850A>T (p.Ser284Cys)
c.77-3529A>T (n.77-3529A>T)
16g.51141081T>CCA395889375SALL1c.1141A>G (p.Ser381Gly)
c.850A>G (p.Ser284Gly)
c.77-3529A>G (n.77-3529A>G)
16g.51141081T>GCA395889376SALL1c.1141A>C (p.Ser381Arg)
c.850A>C (p.Ser284Arg)
c.77-3529A>C (n.77-3529A>C)
16g.51141082T>ACA495781328SALL1c.1140A>T (p.Ile380=)
c.849A>T (p.Ile283=)
c.77-3530A>T (n.77-3530A>T)
16g.51141082T>CCA395889377SALL1c.1140A>G (p.Ile380Met)
c.849A>G (p.Ile283Met)
c.77-3530A>G (n.77-3530A>G)
16g.51141082T>GCA495781330SALL1c.1140A>C (p.Ile380=)
c.849A>C (p.Ile283=)
c.77-3530A>C (n.77-3530A>C)
16g.51141083A>CCA395889378SALL1c.1139T>G (p.Ile380Arg)
c.848T>G (p.Ile283Arg)
c.77-3531T>G (n.77-3531T>G)
16g.51141083A>GCA395889380SALL1c.1139T>C (p.Ile380Thr)
c.848T>C (p.Ile283Thr)
c.77-3531T>C (n.77-3531T>C)
16g.51141083A>TCA395889383SALL1c.1139T>A (p.Ile380Lys)
c.848T>A (p.Ile283Lys)
c.77-3531T>A (n.77-3531T>A)
16g.51141084T>ACA395889385SALL1c.1138A>T (p.Ile380Leu)
c.847A>T (p.Ile283Leu)
c.77-3532A>T (n.77-3532A>T)
16g.51141084T>CCA395889386SALL1c.1138A>G (p.Ile380Val)
c.847A>G (p.Ile283Val)
c.77-3532A>G (n.77-3532A>G)
 dbSNP gnomAD v3 gnomAD v4
16g.51141084T>GCA395889389SALL1c.1138A>C (p.Ile380Leu)
c.847A>C (p.Ile283Leu)
c.77-3532A>C (n.77-3532A>C)
16g.51141084T=CA2222021346SALL1c.1138A= (p.Ile380=)
c.847A= (p.Ile283=)
c.77-3532A= (n.77-3532A=)
16g.51141085T>ACA495781336SALL1c.1137A>T (p.Ala379=)
c.846A>T (p.Ala282=)
c.77-3533A>T (n.77-3533A>T)
16g.51141085T>CCA495781334SALL1c.1137A>G (p.Ala379=)
c.846A>G (p.Ala282=)
c.77-3533A>G (n.77-3533A>G)
16g.51141085T>GCA495781335SALL1c.1137A>C (p.Ala379=)
c.846A>C (p.Ala282=)
c.77-3533A>C (n.77-3533A>C)
16g.51141086G>ACA395889396SALL1c.1136C>T (p.Ala379Val)
c.845C>T (p.Ala282Val)
c.77-3534C>T (n.77-3534C>T)
16g.51141086G>CCA395889395SALL1c.1136C>G (p.Ala379Gly)
c.845C>G (p.Ala282Gly)
c.77-3534C>G (n.77-3534C>G)
16g.51141086G>TCA395889392SALL1c.1136C>A (p.Ala379Glu)
c.845C>A (p.Ala282Glu)
c.77-3534C>A (n.77-3534C>A)
16g.51141087C>ACA395889410SALL1c.1135G>T (p.Ala379Ser)
c.844G>T (p.Ala282Ser)
c.77-3535G>T (n.77-3535G>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.51141087C=CA2222021353SALL1c.1135G= (p.Ala379=)
c.844G= (p.Ala282=)
c.77-3535G= (n.77-3535G=)
16g.51141087C>GCA395889399SALL1c.1135G>C (p.Ala379Pro)
c.844G>C (p.Ala282Pro)
c.77-3535G>C (n.77-3535G>C)
16g.51141087C>TCA395889408SALL1c.1135G>A (p.Ala379Thr)
c.844G>A (p.Ala282Thr)
c.77-3535G>A (n.77-3535G>A)
 dbSNP
16g.51141088A>CCA395889412SALL1c.1134T>G (p.Phe378Leu)
c.843T>G (p.Phe281Leu)
c.77-3536T>G (n.77-3536T>G)
16g.51141088A>GCA495781339SALL1c.1134T>C (p.Phe378=)
c.843T>C (p.Phe281=)
c.77-3536T>C (n.77-3536T>C)
16g.51141088A>TCA395889414SALL1c.1134T>A (p.Phe378Leu)
c.843T>A (p.Phe281Leu)
c.77-3536T>A (n.77-3536T>A)
16g.51141091delCA2695223385SALL1c.1134del (p.Phe378LeufsTer3)
c.843del (p.Phe281LeufsTer3)
c.77-3536del (n.77-3536del)
16g.51141089A=CA2222021357SALL1c.1133T= (p.Phe378=)
c.842T= (p.Phe281=)
c.77-3537T= (n.77-3537T=)
16g.51141089A>CCA395889415SALL1c.1133T>G (p.Phe378Cys)
c.842T>G (p.Phe281Cys)
c.77-3537T>G (n.77-3537T>G)
16g.51141089A>GCA8053333SALL1c.1133T>C (p.Phe378Ser)
c.842T>C (p.Phe281Ser)
c.77-3537T>C (n.77-3537T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141089A>TCA395889416SALL1c.1133T>A (p.Phe378Tyr)
c.842T>A (p.Phe281Tyr)
c.77-3537T>A (n.77-3537T>A)
16g.51141090A>CCA395889418SALL1c.1132T>G (p.Phe378Val)
c.841T>G (p.Phe281Val)
c.77-3538T>G (n.77-3538T>G)
16g.51141090A>GCA395889419SALL1c.1132T>C (p.Phe378Leu)
c.841T>C (p.Phe281Leu)
c.77-3538T>C (n.77-3538T>C)
16g.51141090A>TCA395889422SALL1c.1132T>A (p.Phe378Ile)
c.841T>A (p.Phe281Ile)
c.77-3538T>A (n.77-3538T>A)
16g.51141091A>CCA495781343SALL1c.1131T>G (p.Ala377=)
c.840T>G (p.Ala280=)
c.77-3539T>G (n.77-3539T>G)
16g.51141091A>GCA495781345SALL1c.1131T>C (p.Ala377=)
c.840T>C (p.Ala280=)
c.77-3539T>C (n.77-3539T>C)
16g.51141091A>TCA495781344SALL1c.1131T>A (p.Ala377=)
c.840T>A (p.Ala280=)
c.77-3539T>A (n.77-3539T>A)
16g.51141092G>ACA395889424SALL1c.1130C>T (p.Ala377Val)
c.839C>T (p.Ala280Val)
c.77-3540C>T (n.77-3540C>T)
16g.51141092G>CCA395889425SALL1c.1130C>G (p.Ala377Gly)
c.839C>G (p.Ala280Gly)
c.77-3540C>G (n.77-3540C>G)
 gnomAD v4 COSMIC
16g.51141092G>TCA395889428SALL1c.1130C>A (p.Ala377Asp)
c.839C>A (p.Ala280Asp)
c.77-3540C>A (n.77-3540C>A)
16g.51141093C>ACA395889435SALL1c.1129G>T (p.Ala377Ser)
c.838G>T (p.Ala280Ser)
c.77-3541G>T (n.77-3541G>T)
16g.51141093C>GCA395889431SALL1c.1129G>C (p.Ala377Pro)
c.838G>C (p.Ala280Pro)
c.77-3541G>C (n.77-3541G>C)
16g.51141093C>TCA395889433SALL1c.1129G>A (p.Ala377Thr)
c.838G>A (p.Ala280Thr)
c.77-3541G>A (n.77-3541G>A)
16g.51141094T>ACA495781348SALL1c.1128A>T (p.Pro376=)
c.837A>T (p.Pro279=)
c.77-3542A>T (n.77-3542A>T)
16g.51141094T>CCA495781349SALL1c.1128A>G (p.Pro376=)
c.837A>G (p.Pro279=)
c.77-3542A>G (n.77-3542A>G)
16g.51141094T>GCA495781350SALL1c.1128A>C (p.Pro376=)
c.837A>C (p.Pro279=)
c.77-3542A>C (n.77-3542A>C)
16g.51141095G>ACA395889438SALL1c.1127C>T (p.Pro376Leu)
c.836C>T (p.Pro279Leu)
c.77-3543C>T (n.77-3543C>T)
 gnomAD v4
16g.51141095G>CCA395889446SALL1c.1127C>G (p.Pro376Arg)
c.836C>G (p.Pro279Arg)
c.77-3543C>G (n.77-3543C>G)
16g.51141095G=CA2222021360SALL1c.1127C= (p.Pro376=)
c.836C= (p.Pro279=)
c.77-3543C= (n.77-3543C=)
16g.51141095G>TCA395889447SALL1c.1127C>A (p.Pro376Gln)
c.836C>A (p.Pro279Gln)
c.77-3543C>A (n.77-3543C>A)
 dbSNP
16g.51141096G>ACA395889449SALL1c.1126C>T (p.Pro376Ser)
c.835C>T (p.Pro279Ser)
c.77-3544C>T (n.77-3544C>T)
16g.51141096G>CCA8053334SALL1c.1126C>G (p.Pro376Ala)
c.835C>G (p.Pro279Ala)
c.77-3544C>G (n.77-3544C>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141096G=CA2222021365SALL1c.1126C= (p.Pro376=)
c.835C= (p.Pro279=)
c.77-3544C= (n.77-3544C=)
16g.51141096G>TCA395889456SALL1c.1126C>A (p.Pro376Thr)
c.835C>A (p.Pro279Thr)
c.77-3544C>A (n.77-3544C>A)
16g.51141097T>ACA495781352SALL1c.1125A>T (p.Ser375=)
c.834A>T (p.Ser278=)
c.77-3545A>T (n.77-3545A>T)
16g.51141097T>CCA495781353SALL1c.1125A>G (p.Ser375=)
c.834A>G (p.Ser278=)
c.77-3545A>G (n.77-3545A>G)
16g.51141097T>GCA495781354SALL1c.1125A>C (p.Ser375=)
c.834A>C (p.Ser278=)
c.77-3545A>C (n.77-3545A>C)
 gnomAD v4
16g.51141098delCA2695223387SALL1c.1124del (p.Ser375TyrfsTer6)
c.833del (p.Ser278TyrfsTer6)
c.77-3546del (n.77-3546del)
16g.51141098G>ACA395889458SALL1c.1124C>T (p.Ser375Leu)
c.833C>T (p.Ser278Leu)
c.77-3546C>T (n.77-3546C>T)
 gnomAD v4
16g.51141098G>CCA395889459SALL1c.1124C>G (p.Ser375Ter)
c.833C>G (p.Ser278Ter)
c.77-3546C>G (n.77-3546C>G)
16g.51141098G>TCA395889460SALL1c.1124C>A (p.Ser375Ter)
c.833C>A (p.Ser278Ter)
c.77-3546C>A (n.77-3546C>A)
16g.51141099A>CCA395889461SALL1c.1123T>G (p.Ser375Ala)
c.832T>G (p.Ser278Ala)
c.77-3547T>G (n.77-3547T>G)
16g.51141099A>GCA395889462SALL1c.1123T>C (p.Ser375Pro)
c.832T>C (p.Ser278Pro)
c.77-3547T>C (n.77-3547T>C)
16g.51141099A>TCA395889463SALL1c.1123T>A (p.Ser375Thr)
c.832T>A (p.Ser278Thr)
c.77-3547T>A (n.77-3547T>A)
16g.51141100G>ACA495781360SALL1c.1122C>T (p.Ser374=)
c.831C>T (p.Ser277=)
c.77-3548C>T (n.77-3548C>T)
16g.51141100G>CCA495781361SALL1c.1122C>G (p.Ser374=)
c.831C>G (p.Ser277=)
c.77-3548C>G (n.77-3548C>G)
16g.51141100G>TCA495781359SALL1c.1122C>A (p.Ser374=)
c.831C>A (p.Ser277=)
c.77-3548C>A (n.77-3548C>A)
16g.51141101G>ACA395889466SALL1c.1121C>T (p.Ser374Phe)
c.830C>T (p.Ser277Phe)
c.77-3549C>T (n.77-3549C>T)
16g.51141101G>CCA395889467SALL1c.1121C>G (p.Ser374Cys)
c.830C>G (p.Ser277Cys)
c.77-3549C>G (n.77-3549C>G)
 gnomAD v4
16g.51141101G>TCA395889465SALL1c.1121C>A (p.Ser374Tyr)
c.830C>A (p.Ser277Tyr)
c.77-3549C>A (n.77-3549C>A)
 gnomAD v4
16g.51141102A>CCA395889469SALL1c.1120T>G (p.Ser374Ala)
c.829T>G (p.Ser277Ala)
c.77-3550T>G (n.77-3550T>G)
16g.51141102A>GCA395889472SALL1c.1120T>C (p.Ser374Pro)
c.829T>C (p.Ser277Pro)
c.77-3550T>C (n.77-3550T>C)
16g.51141102A>TCA395889471SALL1c.1120T>A (p.Ser374Thr)
c.829T>A (p.Ser277Thr)
c.77-3550T>A (n.77-3550T>A)
16g.51141103C>ACA495781368SALL1c.1119G>T (p.Ser373=)
c.828G>T (p.Ser276=)
c.77-3551G>T (n.77-3551G>T)
16g.51141103C=CA2222021408SALL1c.1119G= (p.Ser373=)
c.828G= (p.Ser276=)
c.77-3551G= (n.77-3551G=)
16g.51141103C>GCA495781363SALL1c.1119G>C (p.Ser373=)
c.828G>C (p.Ser276=)
c.77-3551G>C (n.77-3551G>C)
 dbSNP gnomAD v2 gnomAD v4
16g.51141103C>TCA8053336SALL1c.1119G>A (p.Ser373=)
c.828G>A (p.Ser276=)
c.77-3551G>A (n.77-3551G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141103_51141106delinsCGATCA2222021412SALL1c.1116_1119delinsATCG (p.Ser372=)
c.825_828delinsATCG (p.Ser275=)
c.77-3554_77-3551delinsATCG (n.77-3554_77-3551delinsATCG)
16g.51141104G>ACA8053337SALL1c.1118C>T (p.Ser373Leu)
c.827C>T (p.Ser276Leu)
c.77-3552C>T (n.77-3552C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.51141104G>CCA395889478SALL1c.1118C>G (p.Ser373Trp)
c.827C>G (p.Ser276Trp)
c.77-3552C>G (n.77-3552C>G)
 dbSNP
16g.51141104G=CA2222021416SALL1c.1118C= (p.Ser373=)
c.827C= (p.Ser276=)
c.77-3552C= (n.77-3552C=)
16g.51141104G>TCA395889481SALL1c.1118C>A (p.Ser373Ter)
c.827C>A (p.Ser276Ter)
c.77-3552C>A (n.77-3552C>A)
16g.51141109_51141111delCA8053335SALL1c.1116_1118del (p.Ser373del)
c.825_827del (p.Ser276del)
c.77-3554_77-3552del (n.77-3554_77-3552del)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141105A>CCA395889484SALL1c.1117T>G (p.Ser373Ala)
c.826T>G (p.Ser276Ala)
c.77-3553T>G (n.77-3553T>G)
16g.51141105A>GCA395889486SALL1c.1117T>C (p.Ser373Pro)
c.826T>C (p.Ser276Pro)
c.77-3553T>C (n.77-3553T>C)
16g.51141105A>TCA395889488SALL1c.1117T>A (p.Ser373Thr)
c.826T>A (p.Ser276Thr)
c.77-3553T>A (n.77-3553T>A)
 COSMIC
16g.51141106T>ACA495781372SALL1c.1116A>T (p.Ser372=)
c.825A>T (p.Ser275=)
c.77-3554A>T (n.77-3554A>T)
16g.51141106T>CCA495781373SALL1c.1116A>G (p.Ser372=)
c.825A>G (p.Ser275=)
c.77-3554A>G (n.77-3554A>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.51141106T>GCA495781374SALL1c.1116A>C (p.Ser372=)
c.825A>C (p.Ser275=)
c.77-3554A>C (n.77-3554A>C)
16g.51141106T=CA2222021419SALL1c.1116A= (p.Ser372=)
c.825A= (p.Ser275=)
c.77-3554A= (n.77-3554A=)
16g.51141107G>ACA395889491SALL1c.1115C>T (p.Ser372Leu)
c.824C>T (p.Ser275Leu)
c.77-3555C>T (n.77-3555C>T)
16g.51141107G>CCA254172SALL1c.1115C>G (p.Ser372Ter)
c.824C>G (p.Ser275Ter)
c.77-3555C>G (n.77-3555C>G)
 ClinVar dbSNP
16g.51141107G=CA2222021433SALL1c.1115C= (p.Ser372=)
c.824C= (p.Ser275=)
c.77-3555C= (n.77-3555C=)
16g.51141107G>TCA254169SALL1c.1115C>A (p.Ser372Ter)
c.824C>A (p.Ser275Ter)
c.77-3555C>A (n.77-3555C>A)
 ClinVar dbSNP
16g.51141108A>CCA395889501SALL1c.1114T>G (p.Ser372Ala)
c.823T>G (p.Ser275Ala)
c.77-3556T>G (n.77-3556T>G)
16g.51141108A>GCA395889499SALL1c.1114T>C (p.Ser372Pro)
c.823T>C (p.Ser275Pro)
c.77-3556T>C (n.77-3556T>C)
16g.51141108A>TCA395889497SALL1c.1114T>A (p.Ser372Thr)
c.823T>A (p.Ser275Thr)
c.77-3556T>A (n.77-3556T>A)
 gnomAD v4
16g.51141109T>ACA495781378SALL1c.1113A>T (p.Ser371=)
c.822A>T (p.Ser274=)
c.77-3557A>T (n.77-3557A>T)
16g.51141109T>CCA495781380SALL1c.1113A>G (p.Ser371=)
c.822A>G (p.Ser274=)
c.77-3557A>G (n.77-3557A>G)
 gnomAD v4
16g.51141109T>GCA495781381SALL1c.1113A>C (p.Ser371=)
c.822A>C (p.Ser274=)
c.77-3557A>C (n.77-3557A>C)
 gnomAD v4
16g.51141110G>ACA8053338SALL1c.1112C>T (p.Ser371Leu)
c.821C>T (p.Ser274Leu)
c.77-3558C>T (n.77-3558C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51141110G>CCA395889508SALL1c.1112C>G (p.Ser371Ter)
c.821C>G (p.Ser274Ter)
c.77-3558C>G (n.77-3558C>G)
 ClinVar
16g.51141110G=CA2222021441SALL1c.1112C= (p.Ser371=)
c.821C= (p.Ser274=)
c.77-3558C= (n.77-3558C=)
16g.51141110G>TCA395889510SALL1c.1112C>A (p.Ser371Ter)
c.821C>A (p.Ser274Ter)
c.77-3558C>A (n.77-3558C>A)
16g.51141111A>CCA395889512SALL1c.1111T>G (p.Ser371Ala)
c.820T>G (p.Ser274Ala)
c.77-3559T>G (n.77-3559T>G)
16g.51141111A>GCA395889513SALL1c.1111T>C (p.Ser371Pro)
c.820T>C (p.Ser274Pro)
c.77-3559T>C (n.77-3559T>C)
16g.51141111A>TCA395889516SALL1c.1111T>A (p.Ser371Thr)
c.820T>A (p.Ser274Thr)
c.77-3559T>A (n.77-3559T>A)
16g.51141112G>ACA495781385SALL1c.1110C>T (p.Val370=)
c.819C>T (p.Val273=)
c.77-3560C>T (n.77-3560C>T)
16g.51141112G>CCA495781386SALL1c.1110C>G (p.Val370=)
c.819C>G (p.Val273=)
c.77-3560C>G (n.77-3560C>G)
 gnomAD v4
16g.51141112G>TCA495781387SALL1c.1110C>A (p.Val370=)
c.819C>A (p.Val273=)
c.77-3560C>A (n.77-3560C>A)
16g.51141112_51141114delinsGACCA2222021452SALL1c.1108_1110delinsGTC (p.Val370=)
c.817_819delinsGTC (p.Val273=)
c.77-3562_77-3560delinsGTC (n.77-3562_77-3560delinsGTC)
16g.51141113A>CCA395889518SALL1c.1109T>G (p.Val370Gly)
c.818T>G (p.Val273Gly)
c.77-3561T>G (n.77-3561T>G)
16g.51141113A>GCA395889520SALL1c.1109T>C (p.Val370Ala)
c.818T>C (p.Val273Ala)
c.77-3561T>C (n.77-3561T>C)
16g.51141113A>TCA395889522SALL1c.1109T>A (p.Val370Asp)
c.818T>A (p.Val273Asp)
c.77-3561T>A (n.77-3561T>A)
16g.51141113_51141114delCA645294090SALL1c.1108_1109del (p.Val370LeufsTer19)
c.817_818del (p.Val273LeufsTer19)
c.77-3562_77-3561del (n.77-3562_77-3561del)
 ClinVar dbSNP
16g.51141114C>ACA395889524SALL1c.1108G>T (p.Val370Phe)
c.817G>T (p.Val273Phe)
c.77-3562G>T (n.77-3562G>T)
16g.51141114C>GCA395889526SALL1c.1108G>C (p.Val370Leu)
c.817G>C (p.Val273Leu)
c.77-3562G>C (n.77-3562G>C)
16g.51141114C>TCA395889528SALL1c.1108G>A (p.Val370Ile)
c.817G>A (p.Val273Ile)
c.77-3562G>A (n.77-3562G>A)
 COSMIC
16g.51141115C>ACA495781392SALL1c.1107G>T (p.Ala369=)
c.816G>T (p.Ala272=)
c.77-3563G>T (n.77-3563G>T)
16g.51141115C=CA2222021459SALL1c.1107G= (p.Ala369=)
c.816G= (p.Ala272=)
c.77-3563G= (n.77-3563G=)
16g.51141115C>GCA495781393SALL1c.1107G>C (p.Ala369=)
c.816G>C (p.Ala272=)
c.77-3563G>C (n.77-3563G>C)
16g.51141115C>TCA8053339SALL1c.1107G>A (p.Ala369=)
c.816G>A (p.Ala272=)
c.77-3563G>A (n.77-3563G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.51141116G>ACA8053340SALL1c.1106C>T (p.Ala369Val)
c.815C>T (p.Ala272Val)
c.77-3564C>T (n.77-3564C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141116G>CCA395889533SALL1c.1106C>G (p.Ala369Gly)
c.815C>G (p.Ala272Gly)
c.77-3564C>G (n.77-3564C>G)
16g.51141116G=CA2222021464SALL1c.1106C= (p.Ala369=)
c.815C= (p.Ala272=)
c.77-3564C= (n.77-3564C=)
16g.51141116G>TCA395889535SALL1c.1106C>A (p.Ala369Glu)
c.815C>A (p.Ala272Glu)
c.77-3564C>A (n.77-3564C>A)
16g.51141117C>ACA395889538SALL1c.1105G>T (p.Ala369Ser)
c.814G>T (p.Ala272Ser)
c.77-3565G>T (n.77-3565G>T)
16g.51141117C>GCA395889540SALL1c.1105G>C (p.Ala369Pro)
c.814G>C (p.Ala272Pro)
c.77-3565G>C (n.77-3565G>C)
16g.51141117C>TCA395889541SALL1c.1105G>A (p.Ala369Thr)
c.814G>A (p.Ala272Thr)
c.77-3565G>A (n.77-3565G>A)
16g.51141118T>ACA495781082SALL1c.1104A>T (p.Pro368=)
c.813A>T (p.Pro271=)
c.77-3566A>T (n.77-3566A>T)
16g.51141118T>CCA495781083SALL1c.1104A>G (p.Pro368=)
c.813A>G (p.Pro271=)
c.77-3566A>G (n.77-3566A>G)
16g.51141118T>GCA495781085SALL1c.1104A>C (p.Pro368=)
c.813A>C (p.Pro271=)
c.77-3566A>C (n.77-3566A>C)
16g.51141119G>ACA395889544SALL1c.1103C>T (p.Pro368Leu)
c.812C>T (p.Pro271Leu)
c.77-3567C>T (n.77-3567C>T)
 gnomAD v4
16g.51141119G>CCA395889545SALL1c.1103C>G (p.Pro368Arg)
c.812C>G (p.Pro271Arg)
c.77-3567C>G (n.77-3567C>G)
16g.51141119G>TCA395889548SALL1c.1103C>A (p.Pro368Gln)
c.812C>A (p.Pro271Gln)
c.77-3567C>A (n.77-3567C>A)
16g.51141120G>ACA395889549SALL1c.1102C>T (p.Pro368Ser)
c.811C>T (p.Pro271Ser)
c.77-3568C>T (n.77-3568C>T)
16g.51141120G>CCA395889552SALL1c.1102C>G (p.Pro368Ala)
c.811C>G (p.Pro271Ala)
c.77-3568C>G (n.77-3568C>G)
16g.51141120G=CA2222021469SALL1c.1102C= (p.Pro368=)
c.811C= (p.Pro271=)
c.77-3568C= (n.77-3568C=)
16g.51141120G>TCA395889553SALL1c.1102C>A (p.Pro368Thr)
c.811C>A (p.Pro271Thr)
c.77-3568C>A (n.77-3568C>A)
 dbSNP
16g.51141121G>ACA495781090SALL1c.1101C>T (p.Asn367=)
c.810C>T (p.Asn270=)
c.77-3569C>T (n.77-3569C>T)
16g.51141121G>CCA395889555SALL1c.1101C>G (p.Asn367Lys)
c.810C>G (p.Asn270Lys)
c.77-3569C>G (n.77-3569C>G)
16g.51141121G>TCA395889557SALL1c.1101C>A (p.Asn367Lys)
c.810C>A (p.Asn270Lys)
c.77-3569C>A (n.77-3569C>A)
 gnomAD v4
16g.51141122T>ACA395889564SALL1c.1100A>T (p.Asn367Ile)
c.809A>T (p.Asn270Ile)
c.77-3570A>T (n.77-3570A>T)
16g.51141122T>CCA395889560SALL1c.1100A>G (p.Asn367Ser)
c.809A>G (p.Asn270Ser)
c.77-3570A>G (n.77-3570A>G)
16g.51141122T>GCA395889562SALL1c.1100A>C (p.Asn367Thr)
c.809A>C (p.Asn270Thr)
c.77-3570A>C (n.77-3570A>C)
16g.51141123T>ACA395889567SALL1c.1099A>T (p.Asn367Tyr)
c.808A>T (p.Asn270Tyr)
c.77-3571A>T (n.77-3571A>T)
16g.51141123T>CCA395889568SALL1c.1099A>G (p.Asn367Asp)
c.808A>G (p.Asn270Asp)
c.77-3571A>G (n.77-3571A>G)
16g.51141123T>GCA395889570SALL1c.1099A>C (p.Asn367His)
c.808A>C (p.Asn270His)
c.77-3571A>C (n.77-3571A>C)
 gnomAD v4
16g.51141124G>ACA495781092SALL1c.1098C>T (p.Ser366=)
c.807C>T (p.Ser269=)
c.77-3572C>T (n.77-3572C>T)
16g.51141124G>CCA395889573SALL1c.1098C>G (p.Ser366Arg)
c.807C>G (p.Ser269Arg)
c.77-3572C>G (n.77-3572C>G)
16g.51141124G>TCA395889576SALL1c.1098C>A (p.Ser366Arg)
c.807C>A (p.Ser269Arg)
c.77-3572C>A (n.77-3572C>A)
16g.51141125C>ACA395889578SALL1c.1097G>T (p.Ser366Ile)
c.806G>T (p.Ser269Ile)
c.77-3573G>T (n.77-3573G>T)
16g.51141125C>GCA395889579SALL1c.1097G>C (p.Ser366Thr)
c.806G>C (p.Ser269Thr)
c.77-3573G>C (n.77-3573G>C)
16g.51141125C>TCA395889580SALL1c.1097G>A (p.Ser366Asn)
c.806G>A (p.Ser269Asn)
c.77-3573G>A (n.77-3573G>A)
16g.51141126T>ACA395889584SALL1c.1096A>T (p.Ser366Cys)
c.805A>T (p.Ser269Cys)
c.77-3574A>T (n.77-3574A>T)
 dbSNP gnomAD v2 gnomAD v4
16g.51141126T>CCA395889586SALL1c.1096A>G (p.Ser366Gly)
c.805A>G (p.Ser269Gly)
c.77-3574A>G (n.77-3574A>G)
16g.51141126T>GCA395889588SALL1c.1096A>C (p.Ser366Arg)
c.805A>C (p.Ser269Arg)
c.77-3574A>C (n.77-3574A>C)
16g.51141126T=CA2222021471SALL1c.1096A= (p.Ser366=)
c.805A= (p.Ser269=)
c.77-3574A= (n.77-3574A=)
16g.51141127G>ACA495781097SALL1c.1095C>T (p.Val365=)
c.804C>T (p.Val268=)
c.77-3575C>T (n.77-3575C>T)
16g.51141127G>CCA495781098SALL1c.1095C>G (p.Val365=)
c.804C>G (p.Val268=)
c.77-3575C>G (n.77-3575C>G)
16g.51141127G>TCA495781099SALL1c.1095C>A (p.Val365=)
c.804C>A (p.Val268=)
c.77-3575C>A (n.77-3575C>A)
16g.51141128A>CCA395889596SALL1c.1094T>G (p.Val365Gly)
c.803T>G (p.Val268Gly)
c.77-3576T>G (n.77-3576T>G)
16g.51141128A>GCA395889594SALL1c.1094T>C (p.Val365Ala)
c.803T>C (p.Val268Ala)
c.77-3576T>C (n.77-3576T>C)
16g.51141128A>TCA395889591SALL1c.1094T>A (p.Val365Asp)
c.803T>A (p.Val268Asp)
c.77-3576T>A (n.77-3576T>A)
16g.51141129C>ACA395889599SALL1c.1093G>T (p.Val365Phe)
c.802G>T (p.Val268Phe)
c.77-3577G>T (n.77-3577G>T)
 dbSNP gnomAD v3 gnomAD v4
16g.51141129C=CA2222021474SALL1c.1093G= (p.Val365=)
c.802G= (p.Val268=)
c.77-3577G= (n.77-3577G=)
16g.51141129C>GCA395889605SALL1c.1093G>C (p.Val365Leu)
c.802G>C (p.Val268Leu)
c.77-3577G>C (n.77-3577G>C)
16g.51141129C>TCA395889602SALL1c.1093G>A (p.Val365Ile)
c.802G>A (p.Val268Ile)
c.77-3577G>A (n.77-3577G>A)
 gnomAD v4
16g.51141130A=CA2222021478SALL1c.1092T= (p.His364=)
c.801T= (p.His267=)
c.77-3578T= (n.77-3578T=)
16g.51141130A>CCA281302731SALL1c.1092T>G (p.His364Gln)
c.801T>G (p.His267Gln)
c.77-3578T>G (n.77-3578T>G)
 dbSNP gnomAD v3 gnomAD v4
16g.51141130A>GCA495781103SALL1c.1092T>C (p.His364=)
c.801T>C (p.His267=)
c.77-3578T>C (n.77-3578T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.51141130A>TCA395889606SALL1c.1092T>A (p.His364Gln)
c.801T>A (p.His267Gln)
c.77-3578T>A (n.77-3578T>A)
16g.51141131T>ACA395889609SALL1c.1091A>T (p.His364Leu)
c.800A>T (p.His267Leu)
c.77-3579A>T (n.77-3579A>T)
16g.51141131T>CCA395889611SALL1c.1091A>G (p.His364Arg)
c.800A>G (p.His267Arg)
c.77-3579A>G (n.77-3579A>G)
 gnomAD v4
16g.51141131T>GCA395889613SALL1c.1091A>C (p.His364Pro)
c.800A>C (p.His267Pro)
c.77-3579A>C (n.77-3579A>C)
 gnomAD v4
16g.51141132G>ACA395889615SALL1c.1090C>T (p.His364Tyr)
c.799C>T (p.His267Tyr)
c.77-3580C>T (n.77-3580C>T)
 gnomAD v4
16g.51141132G>CCA395889616SALL1c.1090C>G (p.His364Asp)
c.799C>G (p.His267Asp)
c.77-3580C>G (n.77-3580C>G)
16g.51141132G>TCA395889619SALL1c.1090C>A (p.His364Asn)
c.799C>A (p.His267Asn)
c.77-3580C>A (n.77-3580C>A)
16g.51141133G>ACA495781107SALL1c.1089C>T (p.Ser363=)
c.798C>T (p.Ser266=)
c.77-3581C>T (n.77-3581C>T)
 dbSNP
16g.51141133G>CCA495781108SALL1c.1089C>G (p.Ser363=)
c.798C>G (p.Ser266=)
c.77-3581C>G (n.77-3581C>G)
16g.51141133G=CA2222021481SALL1c.1089C= (p.Ser363=)
c.798C= (p.Ser266=)
c.77-3581C= (n.77-3581C=)
16g.51141133G>TCA495781109SALL1c.1089C>A (p.Ser363=)
c.798C>A (p.Ser266=)
c.77-3581C>A (n.77-3581C>A)
 dbSNP
16g.51141134G>ACA8053341SALL1c.1088C>T (p.Ser363Phe)
c.797C>T (p.Ser266Phe)
c.77-3582C>T (n.77-3582C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51141134G>CCA395889622SALL1c.1088C>G (p.Ser363Cys)
c.797C>G (p.Ser266Cys)
c.77-3582C>G (n.77-3582C>G)
16g.51141134G=CA2222021482SALL1c.1088C= (p.Ser363=)
c.797C= (p.Ser266=)
c.77-3582C= (n.77-3582C=)
16g.51141134G>TCA395889624SALL1c.1088C>A (p.Ser363Tyr)
c.797C>A (p.Ser266Tyr)
c.77-3582C>A (n.77-3582C>A)
16g.51141135A>CCA395889626SALL1c.1087T>G (p.Ser363Ala)
c.796T>G (p.Ser266Ala)
c.77-3583T>G (n.77-3583T>G)
16g.51141135A>GCA395889627SALL1c.1087T>C (p.Ser363Pro)
c.796T>C (p.Ser266Pro)
c.77-3583T>C (n.77-3583T>C)
16g.51141135A>TCA395889630SALL1c.1087T>A (p.Ser363Thr)
c.796T>A (p.Ser266Thr)
c.77-3583T>A (n.77-3583T>A)
16g.51141136G>ACA8053342SALL1c.1086C>T (p.Ala362=)
c.795C>T (p.Ala265=)
c.77-3584C>T (n.77-3584C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141136G>CCA495781113SALL1c.1086C>G (p.Ala362=)
c.795C>G (p.Ala265=)
c.77-3584C>G (n.77-3584C>G)
16g.51141136G=CA2222021484SALL1c.1086C= (p.Ala362=)
c.795C= (p.Ala265=)
c.77-3584C= (n.77-3584C=)
16g.51141136G>TCA495781114SALL1c.1086C>A (p.Ala362=)
c.795C>A (p.Ala265=)
c.77-3584C>A (n.77-3584C>A)
16g.51141137G>ACA395889632SALL1c.1085C>T (p.Ala362Val)
c.794C>T (p.Ala265Val)
c.77-3585C>T (n.77-3585C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.51141137G>CCA395889636SALL1c.1085C>G (p.Ala362Gly)
c.794C>G (p.Ala265Gly)
c.77-3585C>G (n.77-3585C>G)
16g.51141137G=CA2222021490SALL1c.1085C= (p.Ala362=)
c.794C= (p.Ala265=)
c.77-3585C= (n.77-3585C=)
16g.51141137G>TCA8053343SALL1c.1085C>A (p.Ala362Asp)
c.794C>A (p.Ala265Asp)
c.77-3585C>A (n.77-3585C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51141137_51141138delCA2695223391SALL1c.1084_1085del (p.Ala362LeufsTer27)
c.793_794del (p.Ala265LeufsTer27)
c.77-3586_77-3585del (n.77-3586_77-3585del)
16g.51141138C>ACA395889641SALL1c.1084G>T (p.Ala362Ser)
c.793G>T (p.Ala265Ser)
c.77-3586G>T (n.77-3586G>T)
16g.51141138C>GCA395889644SALL1c.1084G>C (p.Ala362Pro)
c.793G>C (p.Ala265Pro)
c.77-3586G>C (n.77-3586G>C)
16g.51141138C>TCA395889645SALL1c.1084G>A (p.Ala362Thr)
c.793G>A (p.Ala265Thr)
c.77-3586G>A (n.77-3586G>A)
16g.51141139C>ACA495781118SALL1c.1083G>T (p.Gly361=)
c.792G>T (p.Gly264=)
c.77-3587G>T (n.77-3587G>T)
16g.51141139C>GCA495781120SALL1c.1083G>C (p.Gly361=)
c.792G>C (p.Gly264=)
c.77-3587G>C (n.77-3587G>C)
16g.51141139C>TCA495781121SALL1c.1083G>A (p.Gly361=)
c.792G>A (p.Gly264=)
c.77-3587G>A (n.77-3587G>A)
16g.51141140C>ACA395889648SALL1c.1082G>T (p.Gly361Val)
c.791G>T (p.Gly264Val)
c.77-3588G>T (n.77-3588G>T)
16g.51141140C>GCA395889650SALL1c.1082G>C (p.Gly361Ala)
c.791G>C (p.Gly264Ala)
c.77-3588G>C (n.77-3588G>C)
16g.51141140C>TCA395889652SALL1c.1082G>A (p.Gly361Glu)
c.791G>A (p.Gly264Glu)
c.77-3588G>A (n.77-3588G>A)
16g.51141141C>ACA395889654SALL1c.1081G>T (p.Gly361Trp)
c.790G>T (p.Gly264Trp)
c.77-3589G>T (n.77-3589G>T)
16g.51141141C>GCA395889656SALL1c.1081G>C (p.Gly361Arg)
c.790G>C (p.Gly264Arg)
c.77-3589G>C (n.77-3589G>C)
16g.51141141C>TCA395889659SALL1c.1081G>A (p.Gly361Arg)
c.790G>A (p.Gly264Arg)
c.77-3589G>A (n.77-3589G>A)
16g.51141142A>CCA495781127SALL1c.1080T>G (p.Ala360=)
c.789T>G (p.Ala263=)
c.77-3590T>G (n.77-3590T>G)
16g.51141142A>GCA495781125SALL1c.1080T>C (p.Ala360=)
c.789T>C (p.Ala263=)
c.77-3590T>C (n.77-3590T>C)
16g.51141142A>TCA495781124SALL1c.1080T>A (p.Ala360=)
c.789T>A (p.Ala263=)
c.77-3590T>A (n.77-3590T>A)
16g.51141143G>ACA395889666SALL1c.1079C>T (p.Ala360Val)
c.788C>T (p.Ala263Val)
c.77-3591C>T (n.77-3591C>T)
 gnomAD v4
16g.51141143G>CCA395889663SALL1c.1079C>G (p.Ala360Gly)
c.788C>G (p.Ala263Gly)
c.77-3591C>G (n.77-3591C>G)
16g.51141143G>TCA395889662SALL1c.1079C>A (p.Ala360Asp)
c.788C>A (p.Ala263Asp)
c.77-3591C>A (n.77-3591C>A)
16g.51141144C>ACA395889668SALL1c.1078G>T (p.Ala360Ser)
c.787G>T (p.Ala263Ser)
c.77-3592G>T (n.77-3592G>T)
16g.51141144C=CA2222021496SALL1c.1078G= (p.Ala360=)
c.787G= (p.Ala263=)
c.77-3592G= (n.77-3592G=)
16g.51141144C>GCA395889670SALL1c.1078G>C (p.Ala360Pro)
c.787G>C (p.Ala263Pro)
c.77-3592G>C (n.77-3592G>C)
16g.51141144C>TCA395889673SALL1c.1078G>A (p.Ala360Thr)
c.787G>A (p.Ala263Thr)
c.77-3592G>A (n.77-3592G>A)
 dbSNP
16g.51141145A>CCA395889675SALL1c.1077T>G (p.Ser359Arg)
c.786T>G (p.Ser262Arg)
c.77-3593T>G (n.77-3593T>G)
16g.51141145A>GCA495781129SALL1c.1077T>C (p.Ser359=)
c.786T>C (p.Ser262=)
c.77-3593T>C (n.77-3593T>C)
16g.51141145A>TCA395889677SALL1c.1077T>A (p.Ser359Arg)
c.786T>A (p.Ser262Arg)
c.77-3593T>A (n.77-3593T>A)
16g.51141146C>ACA395889680SALL1c.1076G>T (p.Ser359Ile)
c.785G>T (p.Ser262Ile)
c.77-3594G>T (n.77-3594G>T)
16g.51141146C>GCA395889681SALL1c.1076G>C (p.Ser359Thr)
c.785G>C (p.Ser262Thr)
c.77-3594G>C (n.77-3594G>C)
16g.51141146C>TCA395889682SALL1c.1076G>A (p.Ser359Asn)
c.785G>A (p.Ser262Asn)
c.77-3594G>A (n.77-3594G>A)
16g.51141147T>ACA395889685SALL1c.1075A>T (p.Ser359Cys)
c.784A>T (p.Ser262Cys)
c.77-3595A>T (n.77-3595A>T)
16g.51141147T>CCA395889686SALL1c.1075A>G (p.Ser359Gly)
c.784A>G (p.Ser262Gly)
c.77-3595A>G (n.77-3595A>G)
16g.51141147T>GCA395889689SALL1c.1075A>C (p.Ser359Arg)
c.784A>C (p.Ser262Arg)
c.77-3595A>C (n.77-3595A>C)
16g.51141148T>ACA495781133SALL1c.1074A>T (p.Ser358=)
c.783A>T (p.Ser261=)
c.77-3596A>T (n.77-3596A>T)
16g.51141148T>CCA495781135SALL1c.1074A>G (p.Ser358=)
c.783A>G (p.Ser261=)
c.77-3596A>G (n.77-3596A>G)
 gnomAD v4
16g.51141148T>GCA495781134SALL1c.1074A>C (p.Ser358=)
c.783A>C (p.Ser261=)
c.77-3596A>C (n.77-3596A>C)
 gnomAD v4
16g.51141149G>ACA395889698SALL1c.1073C>T (p.Ser358Leu)
c.782C>T (p.Ser261Leu)
c.77-3597C>T (n.77-3597C>T)
 COSMIC
16g.51141149G>CCA395889695SALL1c.1073C>G (p.Ser358Ter)
c.782C>G (p.Ser261Ter)
c.77-3597C>G (n.77-3597C>G)
16g.51141149G>TCA395889693SALL1c.1073C>A (p.Ser358Ter)
c.782C>A (p.Ser261Ter)
c.77-3597C>A (n.77-3597C>A)
16g.51141150A>CCA395889699SALL1c.1072T>G (p.Ser358Ala)
c.781T>G (p.Ser261Ala)
c.77-3598T>G (n.77-3598T>G)
16g.51141150A>GCA395889701SALL1c.1072T>C (p.Ser358Pro)
c.781T>C (p.Ser261Pro)
c.77-3598T>C (n.77-3598T>C)
16g.51141150A>TCA395889703SALL1c.1072T>A (p.Ser358Thr)
c.781T>A (p.Ser261Thr)
c.77-3598T>A (n.77-3598T>A)
16g.51141151A>CCA495781136SALL1c.1071T>G (p.Ala357=)
c.780T>G (p.Ala260=)
c.77-3599T>G (n.77-3599T>G)
16g.51141151A>GCA495781137SALL1c.1071T>C (p.Ala357=)
c.780T>C (p.Ala260=)
c.77-3599T>C (n.77-3599T>C)
16g.51141151A>TCA495781138SALL1c.1071T>A (p.Ala357=)
c.780T>A (p.Ala260=)
c.77-3599T>A (n.77-3599T>A)
16g.51141152G>ACA395889705SALL1c.1070C>T (p.Ala357Val)
c.779C>T (p.Ala260Val)
c.77-3600C>T (n.77-3600C>T)
16g.51141152G>CCA395889707SALL1c.1070C>G (p.Ala357Gly)
c.779C>G (p.Ala260Gly)
c.77-3600C>G (n.77-3600C>G)
16g.51141152G>TCA395889709SALL1c.1070C>A (p.Ala357Asp)
c.779C>A (p.Ala260Asp)
c.77-3600C>A (n.77-3600C>A)
16g.51141153C>ACA395889712SALL1c.1069G>T (p.Ala357Ser)
c.778G>T (p.Ala260Ser)
c.77-3601G>T (n.77-3601G>T)
16g.51141153C>GCA395889715SALL1c.1069G>C (p.Ala357Pro)
c.778G>C (p.Ala260Pro)
c.77-3601G>C (n.77-3601G>C)
 gnomAD v4
16g.51141153C>TCA395889716SALL1c.1069G>A (p.Ala357Thr)
c.778G>A (p.Ala260Thr)
c.77-3601G>A (n.77-3601G>A)
 ClinVar dbSNP
16g.51141154C>ACA495781142SALL1c.1068G>T (p.Val356=)
c.777G>T (p.Val259=)
c.77-3602G>T (n.77-3602G>T)
16g.51141154C>GCA495781141SALL1c.1068G>C (p.Val356=)
c.777G>C (p.Val259=)
c.77-3602G>C (n.77-3602G>C)
16g.51141154C>TCA495781144SALL1c.1068G>A (p.Val356=)
c.777G>A (p.Val259=)
c.77-3602G>A (n.77-3602G>A)
16g.51141155A=CA2222021500SALL1c.1067T= (p.Val356=)
c.776T= (p.Val259=)
c.77-3603T= (n.77-3603T=)
16g.51141155A>CCA395889718SALL1c.1067T>G (p.Val356Gly)
c.776T>G (p.Val259Gly)
c.77-3603T>G (n.77-3603T>G)
16g.51141155A>GCA395889721SALL1c.1067T>C (p.Val356Ala)
c.776T>C (p.Val259Ala)
c.77-3603T>C (n.77-3603T>C)
 dbSNP
16g.51141155A>TCA395889722SALL1c.1067T>A (p.Val356Glu)
c.776T>A (p.Val259Glu)
c.77-3603T>A (n.77-3603T>A)
16g.51141156C>ACA395889726SALL1c.1066G>T (p.Val356Leu)
c.775G>T (p.Val259Leu)
c.77-3604G>T (n.77-3604G>T)
16g.51141156C=CA2222021507SALL1c.1066G= (p.Val356=)
c.775G= (p.Val259=)
c.77-3604G= (n.77-3604G=)
16g.51141156C>GCA395889728SALL1c.1066G>C (p.Val356Leu)
c.775G>C (p.Val259Leu)
c.77-3604G>C (n.77-3604G>C)
 COSMIC
16g.51141156C>TCA395889724SALL1c.1066G>A (p.Val356Met)
c.775G>A (p.Val259Met)
c.77-3604G>A (n.77-3604G>A)
 dbSNP gnomAD v2 gnomAD v4
16g.51141157T>ACA395889734SALL1c.1065A>T (p.Lys355Asn)
c.774A>T (p.Lys258Asn)
c.77-3605A>T (n.77-3605A>T)
16g.51141157T>CCA495781146SALL1c.1065A>G (p.Lys355=)
c.774A>G (p.Lys258=)
c.77-3605A>G (n.77-3605A>G)
 dbSNP gnomAD v2 gnomAD v4
16g.51141157T>GCA395889731SALL1c.1065A>C (p.Lys355Asn)
c.774A>C (p.Lys258Asn)
c.77-3605A>C (n.77-3605A>C)
16g.51141157T=CA2222021513SALL1c.1065A= (p.Lys355=)
c.774A= (p.Lys258=)
c.77-3605A= (n.77-3605A=)
16g.51141161dupCA2695223392SALL1c.1065dup (p.Val356SerfsTer?)
c.774dup (p.Val259SerfsTer?)
c.77-3605dup (n.77-3605dup)
16g.51141158T>ACA395889736SALL1c.1064A>T (p.Lys355Ile)
c.773A>T (p.Lys258Ile)
c.77-3606A>T (n.77-3606A>T)
16g.51141158T>CCA395889739SALL1c.1064A>G (p.Lys355Arg)
c.773A>G (p.Lys258Arg)
c.77-3606A>G (n.77-3606A>G)
16g.51141158T>GCA395889741SALL1c.1064A>C (p.Lys355Thr)
c.773A>C (p.Lys258Thr)
c.77-3606A>C (n.77-3606A>C)
16g.51141159T>ACA395889744SALL1c.1063A>T (p.Lys355Ter)
c.772A>T (p.Lys258Ter)
c.77-3607A>T (n.77-3607A>T)
16g.51141159T>CCA395889745SALL1c.1063A>G (p.Lys355Glu)
c.772A>G (p.Lys258Glu)
c.77-3607A>G (n.77-3607A>G)
16g.51141159T>GCA395889746SALL1c.1063A>C (p.Lys355Gln)
c.772A>C (p.Lys258Gln)
c.77-3607A>C (n.77-3607A>C)
16g.51141160T>ACA395889748SALL1c.1062A>T (p.Glu354Asp)
c.771A>T (p.Glu257Asp)
c.77-3608A>T (n.77-3608A>T)
16g.51141160T>CCA495781148SALL1c.1062A>G (p.Glu354=)
c.771A>G (p.Glu257=)
c.77-3608A>G (n.77-3608A>G)
16g.51141160T>GCA395889751SALL1c.1062A>C (p.Glu354Asp)
c.771A>C (p.Glu257Asp)
c.77-3608A>C (n.77-3608A>C)
16g.51141161T>ACA395889755SALL1c.1061A>T (p.Glu354Val)
c.770A>T (p.Glu257Val)
c.77-3609A>T (n.77-3609A>T)
16g.51141161T>CCA395889758SALL1c.1061A>G (p.Glu354Gly)
c.770A>G (p.Glu257Gly)
c.77-3609A>G (n.77-3609A>G)
16g.51141161T>GCA395889759SALL1c.1061A>C (p.Glu354Ala)
c.770A>C (p.Glu257Ala)
c.77-3609A>C (n.77-3609A>C)
16g.51141162C>ACA395889763SALL1c.1060G>T (p.Glu354Ter)
c.769G>T (p.Glu257Ter)
c.77-3610G>T (n.77-3610G>T)
 COSMIC
16g.51141162C>GCA395889765SALL1c.1060G>C (p.Glu354Gln)
c.769G>C (p.Glu257Gln)
c.77-3610G>C (n.77-3610G>C)
16g.51141162C>TCA395889762SALL1c.1060G>A (p.Glu354Lys)
c.769G>A (p.Glu257Lys)
c.77-3610G>A (n.77-3610G>A)
16g.51141163A>CCA495781151SALL1c.1059T>G (p.Ser353=)
c.768T>G (p.Ser256=)
c.77-3611T>G (n.77-3611T>G)
16g.51141163A>GCA495781152SALL1c.1059T>C (p.Ser353=)
c.768T>C (p.Ser256=)
c.77-3611T>C (n.77-3611T>C)
16g.51141163A>TCA495781153SALL1c.1059T>A (p.Ser353=)
c.768T>A (p.Ser256=)
c.77-3611T>A (n.77-3611T>A)
16g.51141164G>ACA8053344SALL1c.1058C>T (p.Ser353Phe)
c.767C>T (p.Ser256Phe)
c.77-3612C>T (n.77-3612C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51141164G>CCA395889768SALL1c.1058C>G (p.Ser353Cys)
c.767C>G (p.Ser256Cys)
c.77-3612C>G (n.77-3612C>G)
16g.51141164G=CA2222021518SALL1c.1058C= (p.Ser353=)
c.767C= (p.Ser256=)
c.77-3612C= (n.77-3612C=)
16g.51141164G>TCA395889777SALL1c.1058C>A (p.Ser353Tyr)
c.767C>A (p.Ser256Tyr)
c.77-3612C>A (n.77-3612C>A)
16g.51141166_51141168delCA2633181822SALL1c.1056_1058del (p.Ser353del)
c.765_767del (p.Ser256del)
c.77-3614_77-3612del (n.77-3614_77-3612del)
 gnomAD v4
16g.51141165A=CA2222021523SALL1c.1057T= (p.Ser353=)
c.766T= (p.Ser256=)
c.77-3613T= (n.77-3613T=)
16g.51141165A>CCA395889779SALL1c.1057T>G (p.Ser353Ala)
c.766T>G (p.Ser256Ala)
c.77-3613T>G (n.77-3613T>G)
16g.51141165A>GCA395889781SALL1c.1057T>C (p.Ser353Pro)
c.766T>C (p.Ser256Pro)
c.77-3613T>C (n.77-3613T>C)
 dbSNP gnomAD v2 gnomAD v4
16g.51141165A>TCA395889784SALL1c.1057T>A (p.Ser353Thr)
c.766T>A (p.Ser256Thr)
c.77-3613T>A (n.77-3613T>A)
16g.51141166G>ACA8053345SALL1c.1056C>T (p.Ser352=)
c.765C>T (p.Ser255=)
c.77-3614C>T (n.77-3614C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51141166G>CCA495781161SALL1c.1056C>G (p.Ser352=)
c.765C>G (p.Ser255=)
c.77-3614C>G (n.77-3614C>G)
16g.51141166G=CA2222021525SALL1c.1056C= (p.Ser352=)
c.765C= (p.Ser255=)
c.77-3614C= (n.77-3614C=)
16g.51141166G>TCA495781162SALL1c.1056C>A (p.Ser352=)
c.765C>A (p.Ser255=)
c.77-3614C>A (n.77-3614C>A)
16g.51141167G>ACA8053346SALL1c.1055C>T (p.Ser352Phe)
c.764C>T (p.Ser255Phe)
c.77-3615C>T (n.77-3615C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141167G>CCA8053347SALL1c.1055C>G (p.Ser352Cys)
c.764C>G (p.Ser255Cys)
c.77-3615C>G (n.77-3615C>G)
 dbSNP ExAC
16g.51141167G=CA2222021529SALL1c.1055C= (p.Ser352=)
c.764C= (p.Ser255=)
c.77-3615C= (n.77-3615C=)
16g.51141167G>TCA395889792SALL1c.1055C>A (p.Ser352Tyr)
c.764C>A (p.Ser255Tyr)
c.77-3615C>A (n.77-3615C>A)
 gnomAD v4
16g.51141168A>CCA395889801SALL1c.1054T>G (p.Ser352Ala)
c.763T>G (p.Ser255Ala)
c.77-3616T>G (n.77-3616T>G)
16g.51141168A>GCA395889802SALL1c.1054T>C (p.Ser352Pro)
c.763T>C (p.Ser255Pro)
c.77-3616T>C (n.77-3616T>C)
 gnomAD v4
16g.51141168A>TCA395889805SALL1c.1054T>A (p.Ser352Thr)
c.763T>A (p.Ser255Thr)
c.77-3616T>A (n.77-3616T>A)
 gnomAD v4
16g.51141169C>ACA495781164SALL1c.1053G>T (p.Pro351=)
c.762G>T (p.Pro254=)
c.77-3617G>T (n.77-3617G>T)
16g.51141169C=CA2222021531SALL1c.1053G= (p.Pro351=)
c.762G= (p.Pro254=)
c.77-3617G= (n.77-3617G=)
16g.51141169C>GCA495781165SALL1c.1053G>C (p.Pro351=)
c.762G>C (p.Pro254=)
c.77-3617G>C (n.77-3617G>C)
 gnomAD v4
16g.51141169C>TCA281302744SALL1c.1053G>A (p.Pro351=)
c.762G>A (p.Pro254=)
c.77-3617G>A (n.77-3617G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.51141170G>ACA8053348SALL1c.1052C>T (p.Pro351Leu)
c.761C>T (p.Pro254Leu)
c.77-3618C>T (n.77-3618C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141170G>CCA395889810SALL1c.1052C>G (p.Pro351Arg)
c.761C>G (p.Pro254Arg)
c.77-3618C>G (n.77-3618C>G)
16g.51141170G=CA2222021538SALL1c.1052C= (p.Pro351=)
c.761C= (p.Pro254=)
c.77-3618C= (n.77-3618C=)
16g.51141170G>TCA395889807SALL1c.1052C>A (p.Pro351Gln)
c.761C>A (p.Pro254Gln)
c.77-3618C>A (n.77-3618C>A)
16g.51141171G>ACA395889814SALL1c.1051C>T (p.Pro351Ser)
c.760C>T (p.Pro254Ser)
c.77-3619C>T (n.77-3619C>T)
 dbSNP gnomAD v4 COSMIC
16g.51141171G>CCA395889815SALL1c.1051C>G (p.Pro351Ala)
c.760C>G (p.Pro254Ala)
c.77-3619C>G (n.77-3619C>G)
16g.51141171G>TCA395889816SALL1c.1051C>A (p.Pro351Thr)
c.760C>A (p.Pro254Thr)
c.77-3619C>A (n.77-3619C>A)
16g.51141172G>ACA495781167SALL1c.1050C>T (p.Thr350=)
c.759C>T (p.Thr253=)
c.77-3620C>T (n.77-3620C>T)
 dbSNP
16g.51141172G>CCA495781168SALL1c.1050C>G (p.Thr350=)
c.759C>G (p.Thr253=)
c.77-3620C>G (n.77-3620C>G)
16g.51141172G=CA2222021540SALL1c.1050C= (p.Thr350=)
c.759C= (p.Thr253=)
c.77-3620C= (n.77-3620C=)
16g.51141172G>TCA495781169SALL1c.1050C>A (p.Thr350=)
c.759C>A (p.Thr253=)
c.77-3620C>A (n.77-3620C>A)
16g.51141173G>ACA8053349SALL1c.1049C>T (p.Thr350Ile)
c.758C>T (p.Thr253Ile)
c.77-3621C>T (n.77-3621C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141173G>CCA395889820SALL1c.1049C>G (p.Thr350Ser)
c.758C>G (p.Thr253Ser)
c.77-3621C>G (n.77-3621C>G)
16g.51141173G=CA2222021545SALL1c.1049C= (p.Thr350=)
c.758C= (p.Thr253=)
c.77-3621C= (n.77-3621C=)
16g.51141173G>TCA395889823SALL1c.1049C>A (p.Thr350Asn)
c.758C>A (p.Thr253Asn)
c.77-3621C>A (n.77-3621C>A)
16g.51141174T>ACA395889825SALL1c.1048A>T (p.Thr350Ser)
c.757A>T (p.Thr253Ser)
c.77-3622A>T (n.77-3622A>T)
16g.51141174T>CCA395889827SALL1c.1048A>G (p.Thr350Ala)
c.757A>G (p.Thr253Ala)
c.77-3622A>G (n.77-3622A>G)
16g.51141174T>GCA395889829SALL1c.1048A>C (p.Thr350Pro)
c.757A>C (p.Thr253Pro)
c.77-3622A>C (n.77-3622A>C)
16g.51141175G>ACA495781177SALL1c.1047C>T (p.Thr349=)
c.756C>T (p.Thr252=)
c.77-3623C>T (n.77-3623C>T)
16g.51141175G>CCA495781176SALL1c.1047C>G (p.Thr349=)
c.756C>G (p.Thr252=)
c.77-3623C>G (n.77-3623C>G)
16g.51141175G>TCA495781175SALL1c.1047C>A (p.Thr349=)
c.756C>A (p.Thr252=)
c.77-3623C>A (n.77-3623C>A)
16g.51141176dupCA2695223393SALL1c.1047dup (p.Thr350HisfsTer5)
c.756dup (p.Thr253HisfsTer5)
c.77-3623dup (n.77-3623dup)
16g.51141176G>ACA8053350SALL1c.1046C>T (p.Thr349Ile)
c.755C>T (p.Thr252Ile)
c.77-3624C>T (n.77-3624C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51141176G>CCA395889832SALL1c.1046C>G (p.Thr349Ser)
c.755C>G (p.Thr252Ser)
c.77-3624C>G (n.77-3624C>G)
 gnomAD v4
16g.51141176G=CA2222021548SALL1c.1046C= (p.Thr349=)
c.755C= (p.Thr252=)
c.77-3624C= (n.77-3624C=)
16g.51141176G>TCA395889834SALL1c.1046C>A (p.Thr349Asn)
c.755C>A (p.Thr252Asn)
c.77-3624C>A (n.77-3624C>A)
16g.51141177T>ACA395889838SALL1c.1045A>T (p.Thr349Ser)
c.754A>T (p.Thr252Ser)
c.77-3625A>T (n.77-3625A>T)
 dbSNP gnomAD v4
16g.51141177T>CCA395889845SALL1c.1045A>G (p.Thr349Ala)
c.754A>G (p.Thr252Ala)
c.77-3625A>G (n.77-3625A>G)
 gnomAD v4
16g.51141177T>GCA395889837SALL1c.1045A>C (p.Thr349Pro)
c.754A>C (p.Thr252Pro)
c.77-3625A>C (n.77-3625A>C)
16g.51141177T=CA2222021551SALL1c.1045A= (p.Thr349=)
c.754A= (p.Thr252=)
c.77-3625A= (n.77-3625A=)
16g.51141177dupCA2695223395SALL1c.1045dup (p.Thr349AsnfsTer6)
c.754dup (p.Thr252AsnfsTer6)
c.77-3625dup (n.77-3625dup)
16g.51141178A=CA2222021553SALL1c.1044T= (p.Val348=)
c.753T= (p.Val251=)
c.77-3626T= (n.77-3626T=)
16g.51141178A>CCA495781182SALL1c.1044T>G (p.Val348=)
c.753T>G (p.Val251=)
c.77-3626T>G (n.77-3626T>G)
16g.51141178A>GCA495781180SALL1c.1044T>C (p.Val348=)
c.753T>C (p.Val251=)
c.77-3626T>C (n.77-3626T>C)
 dbSNP gnomAD v2 gnomAD v4
16g.51141178A>TCA495781178SALL1c.1044T>A (p.Val348=)
c.753T>A (p.Val251=)
c.77-3626T>A (n.77-3626T>A)

Number of alleles fetched