Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.144413406_144414398delCA2580078692SLC39A4c.1023_1475-7del
c.948_1400-7del
c.1023_1474+117del
c.741_1193-7del
c.741_1192+117del
 ClinVar
8g.144414291delCA2689098465SLC39A4c.1123del (p.Asp375ThrfsTer6)
c.1048del (p.Asp350ThrfsTer6)
c.841del (p.Asp281ThrfsTer6)
 gnomAD v4
8g.144414291C>ACA372621130SLC39A4c.1120G>T (p.Gly374Trp)
c.1045G>T (p.Gly349Trp)
c.838G>T (p.Gly280Trp)
8g.144414291C=CA1826307074SLC39A4c.1120G= (p.Gly374=)
c.1045G= (p.Gly349=)
c.838G= (p.Gly280=)
8g.144414291C>GCA372621131SLC39A4c.1120G>C (p.Gly374Arg)
c.1045G>C (p.Gly349Arg)
c.838G>C (p.Gly280Arg)
8g.144414291C>TCA116333SLC39A4c.1120G>A (p.Gly374Arg)
c.1045G>A (p.Gly349Arg)
c.838G>A (p.Gly280Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414292A>CCA463449601SLC39A4c.1119T>G (p.Thr373=)
c.1044T>G (p.Thr348=)
c.837T>G (p.Thr279=)
8g.144414292A>GCA463449602SLC39A4c.1119T>C (p.Thr373=)
c.1044T>C (p.Thr348=)
c.837T>C (p.Thr279=)
8g.144414292A>TCA463449603SLC39A4c.1119T>A (p.Thr373=)
c.1044T>A (p.Thr348=)
c.837T>A (p.Thr279=)
8g.144414293G>ACA372621133SLC39A4c.1118C>T (p.Thr373Ile)
c.1043C>T (p.Thr348Ile)
c.836C>T (p.Thr279Ile)
 ClinVar
8g.144414293G>CCA4941398SLC39A4c.1118C>G (p.Thr373Ser)
c.1043C>G (p.Thr348Ser)
c.836C>G (p.Thr279Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414293G=CA1826307075SLC39A4c.1118C= (p.Thr373=)
c.1043C= (p.Thr348=)
c.836C= (p.Thr279=)
8g.144414293G>TCA372621132SLC39A4c.1118C>A (p.Thr373Asn)
c.1043C>A (p.Thr348Asn)
c.836C>A (p.Thr279Asn)
 dbSNP gnomAD v3 gnomAD v4
8g.144414294T>ACA372621134SLC39A4c.1117A>T (p.Thr373Ser)
c.1042A>T (p.Thr348Ser)
c.835A>T (p.Thr279Ser)
 gnomAD v4
8g.144414294T>CCA372621135SLC39A4c.1117A>G (p.Thr373Ala)
c.1042A>G (p.Thr348Ala)
c.835A>G (p.Thr279Ala)
 dbSNP gnomAD v4
8g.144414294T>GCA372621136SLC39A4c.1117A>C (p.Thr373Pro)
c.1042A>C (p.Thr348Pro)
c.835A>C (p.Thr279Pro)
8g.144414295G>ACA463449605SLC39A4c.1116C>T (p.Val372=)
c.1041C>T (p.Val347=)
c.1041C>T (p.Leu347=)
c.1116C>T (p.Leu372=)
c.834C>T (p.Val278=)
 gnomAD v4
8g.144414295G>CCA463449606SLC39A4c.1116C>G (p.Val372=)
c.1041C>G (p.Val347=)
c.1041C>G (p.Leu347=)
c.1116C>G (p.Leu372=)
c.834C>G (p.Val278=)
 ClinVar
8g.144414295G>TCA463449607SLC39A4c.1116C>A (p.Val372=)
c.1041C>A (p.Val347=)
c.1041C>A (p.Leu347=)
c.1116C>A (p.Leu372=)
c.834C>A (p.Val278=)
8g.144414296A>CCA372621137SLC39A4c.1115T>G (p.Val372Gly)
c.1040T>G (p.Val347Gly)
c.1040T>G (p.Leu347Arg)
c.1115T>G (p.Leu372Arg)
c.833T>G (p.Val278Gly)
8g.144414296A>GCA372621138SLC39A4c.1115T>C (p.Val372Ala)
c.1040T>C (p.Val347Ala)
c.1040T>C (p.Leu347Pro)
c.1115T>C (p.Leu372Pro)
c.833T>C (p.Val278Ala)
 gnomAD v4
8g.144414296A>TCA372621139SLC39A4c.1115T>A (p.Val372Asp)
c.1040T>A (p.Val347Asp)
c.1040T>A (p.Leu347His)
c.1115T>A (p.Leu372His)
c.833T>A (p.Val278Asp)
8g.144414297delCA2689098480SLC39A4c.1114del (p.Val372SerfsTer9)
c.1039del (p.Val347SerfsTer9)
c.832del (p.Val278SerfsTer9)
 gnomAD v4
8g.144414297C>ACA372621140SLC39A4c.1114G>T (p.Val372Phe)
c.1039G>T (p.Val347Phe)
c.832G>T (p.Val278Phe)
8g.144414297C=CA4941399SLC39A4c.1114G= (p.Val372=)
c.1039G= (p.Val347=)
c.832G= (p.Val278=)
8g.144414297C>GCA187648143SLC39A4c.1114G>C (p.Val372Leu)
c.1039G>C (p.Val347Leu)
c.832G>C (p.Val278Leu)
 dbSNP gnomAD v3 gnomAD v4
8g.144414297C>TCA372621141SLC39A4c.1114G>A (p.Val372Ile)
c.1039G>A (p.Val347Ile)
c.832G>A (p.Val278Ile)
 gnomAD v4
8g.144414297delinsGTGCACCCACAGGACAGCGTCCCCAGTGAGCA2697550211SLC39A4c.1114delinsCTCACTGGGGACGCTGTCCTGTGGGTGCAC (p.Val372LeufsTer19)
c.1039delinsCTCACTGGGGACGCTGTCCTGTGGGTGCAC (p.Val347LeufsTer19)
c.832delinsCTCACTGGGGACGCTGTCCTGTGGGTGCAC (p.Val278LeufsTer19)
 ClinVar
8g.144414298T>ACA463449609SLC39A4c.1113A>T (p.Ala371=)
c.1038A>T (p.Ala346=)
c.831A>T (p.Ala277=)
8g.144414298T>CCA4941400SLC39A4c.1113A>G (p.Ala371=)
c.1038A>G (p.Ala346=)
c.831A>G (p.Ala277=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414298T>GCA463449608SLC39A4c.1113A>C (p.Ala371=)
c.1038A>C (p.Ala346=)
c.831A>C (p.Ala277=)
 gnomAD v4
8g.144414298T=CA1826307076SLC39A4c.1113A= (p.Ala371=)
c.1038A= (p.Ala346=)
c.831A= (p.Ala277=)
8g.144414299G>ACA372621142SLC39A4c.1112C>T (p.Ala371Val)
c.1037C>T (p.Ala346Val)
c.830C>T (p.Ala277Val)
 gnomAD v4
8g.144414299G>CCA372621143SLC39A4c.1112C>G (p.Ala371Gly)
c.1037C>G (p.Ala346Gly)
c.830C>G (p.Ala277Gly)
8g.144414299G>TCA372621144SLC39A4c.1112C>A (p.Ala371Glu)
c.1037C>A (p.Ala346Glu)
c.830C>A (p.Ala277Glu)
 gnomAD v4
8g.144414300C>ACA372621146SLC39A4c.1111G>T (p.Ala371Ser)
c.1036G>T (p.Ala346Ser)
c.829G>T (p.Ala277Ser)
 gnomAD v4
8g.144414300C=CA1826307077SLC39A4c.1111G= (p.Ala371=)
c.1036G= (p.Ala346=)
c.829G= (p.Ala277=)
8g.144414300C>GCA372621147SLC39A4c.1111G>C (p.Ala371Pro)
c.1036G>C (p.Ala346Pro)
c.829G>C (p.Ala277Pro)
8g.144414300C>TCA372621145SLC39A4c.1111G>A (p.Ala371Thr)
c.1036G>A (p.Ala346Thr)
c.829G>A (p.Ala277Thr)
 dbSNP gnomAD v2 gnomAD v4
8g.144414301A=CA1826307079SLC39A4c.1110T= (p.Gly370=)
c.1035T= (p.Gly345=)
c.828T= (p.Gly276=)
8g.144414301A>CCA463449611SLC39A4c.1110T>G (p.Gly370=)
c.1035T>G (p.Gly345=)
c.828T>G (p.Gly276=)
8g.144414301A>GCA463449612SLC39A4c.1110T>C (p.Gly370=)
c.1035T>C (p.Gly345=)
c.828T>C (p.Gly276=)
 ClinVar dbSNP gnomAD v4
8g.144414301A>TCA463449613SLC39A4c.1110T>A (p.Gly370=)
c.1035T>A (p.Gly345=)
c.828T>A (p.Gly276=)
8g.144414301_144414302delinsACCA1826307078SLC39A4c.1109_1110delinsGT (p.Gly370=)
c.1034_1035delinsGT (p.Gly345=)
c.827_828delinsGT (p.Gly276=)
8g.144414302C>ACA372621148SLC39A4c.1109G>T (p.Gly370Val)
c.1034G>T (p.Gly345Val)
c.827G>T (p.Gly276Val)
 gnomAD v4
8g.144414302C>GCA372621149SLC39A4c.1109G>C (p.Gly370Ala)
c.1034G>C (p.Gly345Ala)
c.827G>C (p.Gly276Ala)
 gnomAD v4
8g.144414302C>TCA372621150SLC39A4c.1109G>A (p.Gly370Asp)
c.1034G>A (p.Gly345Asp)
c.827G>A (p.Gly276Asp)
 gnomAD v4
8g.144414304dupCA848876266SLC39A4c.1109dup (p.Ala371CysfsTer?)
c.1034dup (p.Ala346CysfsTer?)
c.827dup (p.Ala277CysfsTer?)
 dbSNP
8g.144414304delCA586164230SLC39A4c.1109del (p.Gly370ValfsTer11)
c.1034del (p.Gly345ValfsTer11)
c.827del (p.Gly276ValfsTer11)
 dbSNP gnomAD v2 gnomAD v4
8g.144414303C>ACA372621151SLC39A4c.1108G>T (p.Gly370Cys)
c.1033G>T (p.Gly345Cys)
c.826G>T (p.Gly276Cys)
 gnomAD v4
8g.144414303C>GCA372621152SLC39A4c.1108G>C (p.Gly370Arg)
c.1033G>C (p.Gly345Arg)
c.826G>C (p.Gly276Arg)
8g.144414303C>TCA372621153SLC39A4c.1108G>A (p.Gly370Ser)
c.1033G>A (p.Gly345Ser)
c.826G>A (p.Gly276Ser)
 gnomAD v4
8g.144414304C>ACA463449614SLC39A4c.1107G>T (p.Val369=)
c.1032G>T (p.Val344=)
c.825G>T (p.Val275=)
 gnomAD v4
8g.144414304C=CA1826307080SLC39A4c.1107G= (p.Val369=)
c.1032G= (p.Val344=)
c.825G= (p.Val275=)
8g.144414304C>GCA463449615SLC39A4c.1107G>C (p.Val369=)
c.1032G>C (p.Val344=)
c.825G>C (p.Val275=)
8g.144414304C>TCA4941401SLC39A4c.1107G>A (p.Val369=)
c.1032G>A (p.Val344=)
c.825G>A (p.Val275=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414305A=CA1826307081SLC39A4c.1106T= (p.Val369=)
c.1031T= (p.Val344=)
c.824T= (p.Val275=)
8g.144414305A>CCA372621154SLC39A4c.1106T>G (p.Val369Gly)
c.1031T>G (p.Val344Gly)
c.824T>G (p.Val275Gly)
8g.144414305A>GCA372621155SLC39A4c.1106T>C (p.Val369Ala)
c.1031T>C (p.Val344Ala)
c.824T>C (p.Val275Ala)
 dbSNP gnomAD v3 gnomAD v4
8g.144414305A>TCA372621156SLC39A4c.1106T>A (p.Val369Glu)
c.1031T>A (p.Val344Glu)
c.824T>A (p.Val275Glu)
8g.144414306C>ACA372621157SLC39A4c.1105G>T (p.Val369Leu)
c.1030G>T (p.Val344Leu)
c.823G>T (p.Val275Leu)
8g.144414306C>GCA372621158SLC39A4c.1105G>C (p.Val369Leu)
c.1030G>C (p.Val344Leu)
c.823G>C (p.Val275Leu)
8g.144414306C>TCA372621159SLC39A4c.1105G>A (p.Val369Met)
c.1030G>A (p.Val344Met)
c.823G>A (p.Val275Met)
 gnomAD v4
8g.144414307T>ACA463449622SLC39A4c.1104A>T (p.Ala368=)
c.1029A>T (p.Ala343=)
c.822A>T (p.Ala274=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414307T>CCA463449621SLC39A4c.1104A>G (p.Ala368=)
c.1029A>G (p.Ala343=)
c.822A>G (p.Ala274=)
8g.144414307T>GCA463449620SLC39A4c.1104A>C (p.Ala368=)
c.1029A>C (p.Ala343=)
c.822A>C (p.Ala274=)
8g.144414307T=CA1826307082SLC39A4c.1104A= (p.Ala368=)
c.1029A= (p.Ala343=)
c.822A= (p.Ala274=)
8g.144414308G>ACA4941402SLC39A4c.1103C>T (p.Ala368Val)
c.1028C>T (p.Ala343Val)
c.821C>T (p.Ala274Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414308G>CCA372621161SLC39A4c.1103C>G (p.Ala368Gly)
c.1028C>G (p.Ala343Gly)
c.821C>G (p.Ala274Gly)
8g.144414308G=CA1826307083SLC39A4c.1103C= (p.Ala368=)
c.1028C= (p.Ala343=)
c.821C= (p.Ala274=)
8g.144414308G>TCA372621160SLC39A4c.1103C>A (p.Ala368Glu)
c.1028C>A (p.Ala343Glu)
c.821C>A (p.Ala274Glu)
 gnomAD v4
8g.144414309C>ACA372621162SLC39A4c.1102G>T (p.Ala368Ser)
c.1027G>T (p.Ala343Ser)
c.820G>T (p.Ala274Ser)
 gnomAD v4
8g.144414309C>GCA372621163SLC39A4c.1102G>C (p.Ala368Pro)
c.1027G>C (p.Ala343Pro)
c.820G>C (p.Ala274Pro)
8g.144414309C>TCA372621164SLC39A4c.1102G>A (p.Ala368Thr)
c.1027G>A (p.Ala343Thr)
c.820G>A (p.Ala274Thr)
 gnomAD v4
8g.144414310C>ACA463449623SLC39A4c.1101G>T (p.Leu367=)
c.1026G>T (p.Leu342=)
c.819G>T (p.Leu273=)
 dbSNP gnomAD v3 gnomAD v4
8g.144414310C=CA1826307084SLC39A4c.1101G= (p.Leu367=)
c.1026G= (p.Leu342=)
c.819G= (p.Leu273=)
8g.144414310C>GCA463449624SLC39A4c.1101G>C (p.Leu367=)
c.1026G>C (p.Leu342=)
c.819G>C (p.Leu273=)
8g.144414310C>TCA4941403SLC39A4c.1101G>A (p.Leu367=)
c.1026G>A (p.Leu342=)
c.819G>A (p.Leu273=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414311A>CCA372621165SLC39A4c.1100T>G (p.Leu367Arg)
c.1025T>G (p.Leu342Arg)
c.818T>G (p.Leu273Arg)
8g.144414311A>GCA372621166SLC39A4c.1100T>C (p.Leu367Pro)
c.1025T>C (p.Leu342Pro)
c.818T>C (p.Leu273Pro)
8g.144414311A>TCA372621167SLC39A4c.1100T>A (p.Leu367Gln)
c.1025T>A (p.Leu342Gln)
c.818T>A (p.Leu273Gln)
8g.144414312G>ACA463449625SLC39A4c.1099C>T (p.Leu367=)
c.1024C>T (p.Leu342=)
c.817C>T (p.Leu273=)
8g.144414312G>CCA372621168SLC39A4c.1099C>G (p.Leu367Val)
c.1024C>G (p.Leu342Val)
c.817C>G (p.Leu273Val)
8g.144414312G>TCA372621169SLC39A4c.1099C>A (p.Leu367Met)
c.1024C>A (p.Leu342Met)
c.817C>A (p.Leu273Met)
8g.144414313G>ACA463449626SLC39A4c.1098C>T (p.Ser366=)
c.1023C>T (p.Ser341=)
c.816C>T (p.Ser272=)
 gnomAD v4
8g.144414313G>CCA372621170SLC39A4c.1098C>G (p.Ser366Arg)
c.1023C>G (p.Ser341Arg)
c.816C>G (p.Ser272Arg)
 gnomAD v4
8g.144414313G>TCA372621171SLC39A4c.1098C>A (p.Ser366Arg)
c.1023C>A (p.Ser341Arg)
c.816C>A (p.Ser272Arg)
 COSMIC COSMIC
8g.144414314C>ACA372621173SLC39A4c.1097G>T (p.Ser366Ile)
c.1022G>T (p.Ser341Ile)
c.815G>T (p.Ser272Ile)
8g.144414314C=CA1826307085SLC39A4c.1097G= (p.Ser366=)
c.1022G= (p.Ser341=)
c.815G= (p.Ser272=)
8g.144414314C>GCA372621174SLC39A4c.1097G>C (p.Ser366Thr)
c.1022G>C (p.Ser341Thr)
c.815G>C (p.Ser272Thr)
8g.144414314C>TCA372621172SLC39A4c.1097G>A (p.Ser366Asn)
c.1022G>A (p.Ser341Asn)
c.815G>A (p.Ser272Asn)
 dbSNP gnomAD v4
8g.144414315T>ACA372621175SLC39A4c.1096A>T (p.Ser366Cys)
c.1021A>T (p.Ser341Cys)
c.814A>T (p.Ser272Cys)
8g.144414315T>CCA372621176SLC39A4c.1096A>G (p.Ser366Gly)
c.1021A>G (p.Ser341Gly)
c.814A>G (p.Ser272Gly)
8g.144414315T>GCA372621177SLC39A4c.1096A>C (p.Ser366Arg)
c.1021A>C (p.Ser341Arg)
c.814A>C (p.Ser272Arg)
8g.144414316C>ACA463449631SLC39A4c.1095G>T (p.Leu365=)
c.1020G>T (p.Leu340=)
c.813G>T (p.Leu271=)
8g.144414316C>GCA463449632SLC39A4c.1095G>C (p.Leu365=)
c.1020G>C (p.Leu340=)
c.813G>C (p.Leu271=)
8g.144414316C>TCA463449633SLC39A4c.1095G>A (p.Leu365=)
c.1020G>A (p.Leu340=)
c.813G>A (p.Leu271=)
 gnomAD v4
8g.144414321_144414332delCA2689098548SLC39A4c.1084_1095del (p.Gln362_Leu365del)
c.1009_1020del (p.Gln337_Leu340del)
c.802_813del (p.Gln268_Leu271del)
 gnomAD v4
8g.144414317A>CCA372621178SLC39A4c.1094T>G (p.Leu365Arg)
c.1019T>G (p.Leu340Arg)
c.812T>G (p.Leu271Arg)
8g.144414317A>GCA372621179SLC39A4c.1094T>C (p.Leu365Pro)
c.1019T>C (p.Leu340Pro)
c.812T>C (p.Leu271Pro)
 gnomAD v4
8g.144414317A>TCA372621180SLC39A4c.1094T>A (p.Leu365Gln)
c.1019T>A (p.Leu340Gln)
c.812T>A (p.Leu271Gln)
8g.144414318G>ACA463449634SLC39A4c.1093C>T (p.Leu365=)
c.1018C>T (p.Leu340=)
c.811C>T (p.Leu271=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
8g.144414318G>CCA372621181SLC39A4c.1093C>G (p.Leu365Val)
c.1018C>G (p.Leu340Val)
c.811C>G (p.Leu271Val)
8g.144414318G=CA1826307086SLC39A4c.1093C= (p.Leu365=)
c.1018C= (p.Leu340=)
c.811C= (p.Leu271=)
8g.144414318G>TCA372621182SLC39A4c.1093C>A (p.Leu365Met)
c.1018C>A (p.Leu340Met)
c.811C>A (p.Leu271Met)
 gnomAD v4
8g.144414319G>ACA463449635SLC39A4c.1092C>T (p.Phe364=)
c.1017C>T (p.Phe339=)
c.810C>T (p.Phe270=)
8g.144414319G>CCA372621183SLC39A4c.1092C>G (p.Phe364Leu)
c.1017C>G (p.Phe339Leu)
c.810C>G (p.Phe270Leu)
8g.144414319G>TCA372621184SLC39A4c.1092C>A (p.Phe364Leu)
c.1017C>A (p.Phe339Leu)
c.810C>A (p.Phe270Leu)
8g.144414320A>CCA372621185SLC39A4c.1091T>G (p.Phe364Cys)
c.1016T>G (p.Phe339Cys)
c.809T>G (p.Phe270Cys)
8g.144414320A>GCA372621186SLC39A4c.1091T>C (p.Phe364Ser)
c.1016T>C (p.Phe339Ser)
c.809T>C (p.Phe270Ser)
8g.144414320A>TCA372621187SLC39A4c.1091T>A (p.Phe364Tyr)
c.1016T>A (p.Phe339Tyr)
c.809T>A (p.Phe270Tyr)
8g.144414321A=CA1826307087SLC39A4c.1090T= (p.Phe364=)
c.1015T= (p.Phe339=)
c.808T= (p.Phe270=)
8g.144414321A>CCA372621190SLC39A4c.1090T>G (p.Phe364Val)
c.1015T>G (p.Phe339Val)
c.808T>G (p.Phe270Val)
8g.144414321A>GCA372621189SLC39A4c.1090T>C (p.Phe364Leu)
c.1015T>C (p.Phe339Leu)
c.808T>C (p.Phe270Leu)
 dbSNP gnomAD v2 gnomAD v4
8g.144414321A>TCA372621188SLC39A4c.1090T>A (p.Phe364Ile)
c.1015T>A (p.Phe339Ile)
c.808T>A (p.Phe270Ile)
8g.144414322G>ACA4941404SLC39A4c.1089C>T (p.Thr363=)
c.1014C>T (p.Thr338=)
c.807C>T (p.Thr269=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414322G>CCA463449640SLC39A4c.1089C>G (p.Thr363=)
c.1014C>G (p.Thr338=)
c.807C>G (p.Thr269=)
8g.144414322G=CA1826307088SLC39A4c.1089C= (p.Thr363=)
c.1014C= (p.Thr338=)
c.807C= (p.Thr269=)
8g.144414322G>TCA463449639SLC39A4c.1089C>A (p.Thr363=)
c.1014C>A (p.Thr338=)
c.807C>A (p.Thr269=)
 gnomAD v4
8g.144414323dupCA1139660828SLC39A4c.1089dup (p.Phe364LeufsTer?)
c.1014dup (p.Phe339LeufsTer?)
c.807dup (p.Phe270LeufsTer?)
 ClinVar dbSNP
8g.144414323G>ACA372621191SLC39A4c.1088C>T (p.Thr363Ile)
c.1013C>T (p.Thr338Ile)
c.806C>T (p.Thr269Ile)
 dbSNP
8g.144414323G>CCA372621192SLC39A4c.1088C>G (p.Thr363Ser)
c.1013C>G (p.Thr338Ser)
c.806C>G (p.Thr269Ser)
 dbSNP gnomAD v4
8g.144414323G=CA1826307089SLC39A4c.1088C= (p.Thr363=)
c.1013C= (p.Thr338=)
c.806C= (p.Thr269=)
8g.144414323G>TCA372621193SLC39A4c.1088C>A (p.Thr363Asn)
c.1013C>A (p.Thr338Asn)
c.806C>A (p.Thr269Asn)
 dbSNP gnomAD v2 gnomAD v4
8g.144414324T>ACA372621194SLC39A4c.1087A>T (p.Thr363Ser)
c.1012A>T (p.Thr338Ser)
c.805A>T (p.Thr269Ser)
 gnomAD v4
8g.144414324T>CCA372621195SLC39A4c.1087A>G (p.Thr363Ala)
c.1012A>G (p.Thr338Ala)
c.805A>G (p.Thr269Ala)
8g.144414324T>GCA372621196SLC39A4c.1087A>C (p.Thr363Pro)
c.1012A>C (p.Thr338Pro)
c.805A>C (p.Thr269Pro)
8g.144414325C>ACA372621197SLC39A4c.1086G>T (p.Gln362His)
c.1011G>T (p.Gln337His)
c.804G>T (p.Gln268His)
 gnomAD v4
8g.144414325C>GCA372621198SLC39A4c.1086G>C (p.Gln362His)
c.1011G>C (p.Gln337His)
c.804G>C (p.Gln268His)
8g.144414325C>TCA463449641SLC39A4c.1086G>A (p.Gln362=)
c.1011G>A (p.Gln337=)
c.804G>A (p.Gln268=)
 gnomAD v4
8g.144414326T>ACA372621199SLC39A4c.1085A>T (p.Gln362Leu)
c.1010A>T (p.Gln337Leu)
c.803A>T (p.Gln268Leu)
8g.144414326T>CCA372621200SLC39A4c.1085A>G (p.Gln362Arg)
c.1010A>G (p.Gln337Arg)
c.803A>G (p.Gln268Arg)
 gnomAD v4
8g.144414326T>GCA372621201SLC39A4c.1085A>C (p.Gln362Pro)
c.1010A>C (p.Gln337Pro)
c.803A>C (p.Gln268Pro)
8g.144414327G>ACA372621202SLC39A4c.1084C>T (p.Gln362Ter)
c.1009C>T (p.Gln337Ter)
c.802C>T (p.Gln268Ter)
 dbSNP gnomAD v2 gnomAD v4
8g.144414327G>CCA372621203SLC39A4c.1084C>G (p.Gln362Glu)
c.1009C>G (p.Gln337Glu)
c.802C>G (p.Gln268Glu)
8g.144414327G=CA1826307090SLC39A4c.1084C= (p.Gln362=)
c.1009C= (p.Gln337=)
c.802C= (p.Gln268=)
8g.144414327G>TCA372621204SLC39A4c.1084C>A (p.Gln362Lys)
c.1009C>A (p.Gln337Lys)
c.802C>A (p.Gln268Lys)
8g.144414328C>ACA463449642SLC39A4c.1083G>T (p.Leu361=)
c.1008G>T (p.Leu336=)
c.801G>T (p.Leu267=)
 gnomAD v4
8g.144414328C>GCA463449643SLC39A4c.1083G>C (p.Leu361=)
c.1008G>C (p.Leu336=)
c.801G>C (p.Leu267=)
8g.144414328C>TCA463449644SLC39A4c.1083G>A (p.Leu361=)
c.1008G>A (p.Leu336=)
c.801G>A (p.Leu267=)
 gnomAD v4
8g.144414329A>CCA372621206SLC39A4c.1082T>G (p.Leu361Arg)
c.1007T>G (p.Leu336Arg)
c.800T>G (p.Leu267Arg)
8g.144414329A>GCA372621207SLC39A4c.1082T>C (p.Leu361Pro)
c.1007T>C (p.Leu336Pro)
c.800T>C (p.Leu267Pro)
 gnomAD v4
8g.144414329A>TCA372621205SLC39A4c.1082T>A (p.Leu361Gln)
c.1007T>A (p.Leu336Gln)
c.800T>A (p.Leu267Gln)
 gnomAD v4
8g.144414330G>ACA463449648SLC39A4c.1081C>T (p.Leu361=)
c.1006C>T (p.Leu336=)
c.799C>T (p.Leu267=)
 dbSNP gnomAD v4
8g.144414330G>CCA372621208SLC39A4c.1081C>G (p.Leu361Val)
c.1006C>G (p.Leu336Val)
c.799C>G (p.Leu267Val)
8g.144414330G=CA1826307091SLC39A4c.1081C= (p.Leu361=)
c.1006C= (p.Leu336=)
c.799C= (p.Leu267=)
8g.144414330G>TCA372621209SLC39A4c.1081C>A (p.Leu361Met)
c.1006C>A (p.Leu336Met)
c.799C>A (p.Leu267Met)
 gnomAD v4
8g.144414331G>ACA463449650SLC39A4c.1080C>T (p.Ile360=)
c.1005C>T (p.Ile335=)
c.798C>T (p.Ile266=)
 ClinVar dbSNP gnomAD v2
8g.144414331G>CCA4941405SLC39A4c.1080C>G (p.Ile360Met)
c.1005C>G (p.Ile335Met)
c.798C>G (p.Ile266Met)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414331G=CA1826307092SLC39A4c.1080C= (p.Ile360=)
c.1005C= (p.Ile335=)
c.798C= (p.Ile266=)
8g.144414331G>TCA463449649SLC39A4c.1080C>A (p.Ile360=)
c.1005C>A (p.Ile335=)
c.798C>A (p.Ile266=)
8g.144414332A=CA1826307093SLC39A4c.1079T= (p.Ile360=)
c.1004T= (p.Ile335=)
c.797T= (p.Ile266=)
8g.144414332A>CCA372621210SLC39A4c.1079T>G (p.Ile360Ser)
c.1004T>G (p.Ile335Ser)
c.797T>G (p.Ile266Ser)
8g.144414332A>GCA372621211SLC39A4c.1079T>C (p.Ile360Thr)
c.1004T>C (p.Ile335Thr)
c.797T>C (p.Ile266Thr)
 gnomAD v4
8g.144414332A>TCA4941406SLC39A4c.1079T>A (p.Ile360Asn)
c.1004T>A (p.Ile335Asn)
c.797T>A (p.Ile266Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414333T>ACA372621214SLC39A4c.1078A>T (p.Ile360Phe)
c.1003A>T (p.Ile335Phe)
c.796A>T (p.Ile266Phe)
 gnomAD v4
8g.144414333T>CCA372621212SLC39A4c.1078A>G (p.Ile360Val)
c.1003A>G (p.Ile335Val)
c.796A>G (p.Ile266Val)
 dbSNP gnomAD v4
8g.144414333T>GCA372621213SLC39A4c.1078A>C (p.Ile360Leu)
c.1003A>C (p.Ile335Leu)
c.796A>C (p.Ile266Leu)
8g.144414333T=CA1826307094SLC39A4c.1078A= (p.Ile360=)
c.1003A= (p.Ile335=)
c.796A= (p.Ile266=)
8g.144414334G>ACA463449651SLC39A4c.1077C>T (p.Tyr359=)
c.1002C>T (p.Tyr334=)
c.795C>T (p.Tyr265=)
 ClinVar dbSNP gnomAD v4
8g.144414334G>CCA372621215SLC39A4c.1077C>G (p.Tyr359Ter)
c.1002C>G (p.Tyr334Ter)
c.795C>G (p.Tyr265Ter)
8g.144414334G=CA1826307095SLC39A4c.1077C= (p.Tyr359=)
c.1002C= (p.Tyr334=)
c.795C= (p.Tyr265=)
8g.144414334G>TCA372621216SLC39A4c.1077C>A (p.Tyr359Ter)
c.1002C>A (p.Tyr334Ter)
c.795C>A (p.Tyr265Ter)
 gnomAD v4
8g.144414335T>ACA372621217SLC39A4c.1076A>T (p.Tyr359Phe)
c.1001A>T (p.Tyr334Phe)
c.794A>T (p.Tyr265Phe)
8g.144414335T>CCA372621218SLC39A4c.1076A>G (p.Tyr359Cys)
c.1001A>G (p.Tyr334Cys)
c.794A>G (p.Tyr265Cys)
 dbSNP gnomAD v2 gnomAD v4
8g.144414335T>GCA372621219SLC39A4c.1076A>C (p.Tyr359Ser)
c.1001A>C (p.Tyr334Ser)
c.794A>C (p.Tyr265Ser)
8g.144414335T=CA1826307096SLC39A4c.1076A= (p.Tyr359=)
c.1001A= (p.Tyr334=)
c.794A= (p.Tyr265=)
8g.144414336A>CCA372621220SLC39A4c.1075T>G (p.Tyr359Asp)
c.1000T>G (p.Tyr334Asp)
c.793T>G (p.Tyr265Asp)
8g.144414336A>GCA372621222SLC39A4c.1075T>C (p.Tyr359His)
c.1000T>C (p.Tyr334His)
c.793T>C (p.Tyr265His)
8g.144414336A>TCA372621221SLC39A4c.1075T>A (p.Tyr359Asn)
c.1000T>A (p.Tyr334Asn)
c.793T>A (p.Tyr265Asn)
8g.144414337G>ACA4941407SLC39A4c.1074C>T (p.His358=)
c.999C>T (p.His333=)
c.792C>T (p.His264=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414337G>CCA372621223SLC39A4c.1074C>G (p.His358Gln)
c.999C>G (p.His333Gln)
c.792C>G (p.His264Gln)
8g.144414337G=CA1826307097SLC39A4c.1074C= (p.His358=)
c.999C= (p.His333=)
c.792C= (p.His264=)
8g.144414337G>TCA372621224SLC39A4c.1074C>A (p.His358Gln)
c.999C>A (p.His333Gln)
c.792C>A (p.His264Gln)
8g.144414338T>ACA372621225SLC39A4c.1073A>T (p.His358Leu)
c.998A>T (p.His333Leu)
c.791A>T (p.His264Leu)
8g.144414338T>CCA372621226SLC39A4c.1073A>G (p.His358Arg)
c.998A>G (p.His333Arg)
c.791A>G (p.His264Arg)
 dbSNP gnomAD v4
8g.144414338T>GCA372621227SLC39A4c.1073A>C (p.His358Pro)
c.998A>C (p.His333Pro)
c.791A>C (p.His264Pro)
8g.144414338T=CA1826307098SLC39A4c.1073A= (p.His358=)
c.998A= (p.His333=)
c.791A= (p.His264=)
8g.144414339G>ACA372621228SLC39A4c.1072C>T (p.His358Tyr)
c.997C>T (p.His333Tyr)
c.790C>T (p.His264Tyr)
 dbSNP gnomAD v2 gnomAD v4
8g.144414339G>CCA372621229SLC39A4c.1072C>G (p.His358Asp)
c.997C>G (p.His333Asp)
c.790C>G (p.His264Asp)
8g.144414339G=CA1826307099SLC39A4c.1072C= (p.His358=)
c.997C= (p.His333=)
c.790C= (p.His264=)
8g.144414339G>TCA372621230SLC39A4c.1072C>A (p.His358Asn)
c.997C>A (p.His333Asn)
c.790C>A (p.His264Asn)
8g.144414340G>ACA463449655SLC39A4c.1071C>T (p.Thr357=)
c.996C>T (p.Thr332=)
c.789C>T (p.Thr263=)
 dbSNP gnomAD v2
8g.144414340G>CCA463449657SLC39A4c.1071C>G (p.Thr357=)
c.996C>G (p.Thr332=)
c.789C>G (p.Thr263=)
 ClinVar gnomAD v4
8g.144414340G=CA1826307100SLC39A4c.1071C= (p.Thr357=)
c.996C= (p.Thr332=)
c.789C= (p.Thr263=)
8g.144414340G>TCA463449656SLC39A4c.1071C>A (p.Thr357=)
c.996C>A (p.Thr332=)
c.789C>A (p.Thr263=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
8g.144414340_144414341insTACA2689098692SLC39A4c.1070_1071insTA (p.His358ThrfsTer9)
c.995_996insTA (p.His333ThrfsTer9)
c.788_789insTA (p.His264ThrfsTer9)
 gnomAD v4
8g.144414341G>ACA4941408SLC39A4c.1070C>T (p.Thr357Ile)
c.995C>T (p.Thr332Ile)
c.788C>T (p.Thr263Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414341G>CCA372621231SLC39A4c.1070C>G (p.Thr357Ser)
c.995C>G (p.Thr332Ser)
c.788C>G (p.Thr263Ser)
8g.144414341G=CA1826307101SLC39A4c.1070C= (p.Thr357=)
c.995C= (p.Thr332=)
c.788C= (p.Thr263=)
8g.144414341G>TCA372621232SLC39A4c.1070C>A (p.Thr357Asn)
c.995C>A (p.Thr332Asn)
c.788C>A (p.Thr263Asn)
8g.144414342_144414394dupCA2580078709SLC39A4c.1018_1070dup (p.His358AlafsTer9)
c.943_995dup (p.His333AlafsTer9)
c.736_788dup (p.His264AlafsTer9)
 ClinVar dbSNP
8g.144414342T>ACA372621234SLC39A4c.1069A>T (p.Thr357Ser)
c.994A>T (p.Thr332Ser)
c.787A>T (p.Thr263Ser)
 dbSNP gnomAD v4
8g.144414342T>CCA4941409SLC39A4c.1069A>G (p.Thr357Ala)
c.994A>G (p.Thr332Ala)
c.787A>G (p.Thr263Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414342T>GCA372621233SLC39A4c.1069A>C (p.Thr357Pro)
c.994A>C (p.Thr332Pro)
c.787A>C (p.Thr263Pro)
8g.144414342T=CA1826307102SLC39A4c.1069A= (p.Thr357=)
c.994A= (p.Thr332=)
c.787A= (p.Thr263=)
8g.144414342_144414343delinsCACA2499219171SLC39A4c.1068_1069delinsTG (p.Thr357Ala)
c.993_994delinsTG (p.Thr332Ala)
c.786_787delinsTG (p.Thr263Ala)
 ClinVar
8g.144414343G>ACA4941410SLC39A4c.1068C>T (p.Val356=)
c.993C>T (p.Val331=)
c.786C>T (p.Val262=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414343G>CCA463449659SLC39A4c.1068C>G (p.Val356=)
c.993C>G (p.Val331=)
c.786C>G (p.Val262=)
8g.144414343G=CA1826307103SLC39A4c.1068C= (p.Val356=)
c.993C= (p.Val331=)
c.786C= (p.Val262=)
8g.144414343G>TCA463449660SLC39A4c.1068C>A (p.Val356=)
c.993C>A (p.Val331=)
c.786C>A (p.Val262=)
8g.144414343_144414344insGGCGCA2689098723SLC39A4c.1068_1069insGCCC (p.Thr357AlafsTer?)
c.993_994insGCCC (p.Thr332AlafsTer?)
c.786_787insGCCC (p.Thr263AlafsTer?)
 gnomAD v4
8g.144414376_144414377insGCCAGGCTCAGGAAGGTCTGCAGGATGTAGTGGGCGACCCCCCTGCAGCCAGTGCAGGTCAGCAGCAGGCA2512985975SLC39A4c.1068_1069insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC (p.Val356_Thr357insAlaHisTyrIleLeuGlnThrPheLeuSerLeuAlaLeuLeuLeuThrCysThrGlyCysArgGlyVal)
c.993_994insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC (p.Val331_Thr332insAlaHisTyrIleLeuGlnThrPheLeuSerLeuAlaLeuLeuLeuThrCysThrGlyCysArgGlyVal)
c.786_787insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC (p.Val262_Thr263insAlaHisTyrIleLeuGlnThrPheLeuSerLeuAlaLeuLeuLeuThrCysThrGlyCysArgGlyVal)
8g.144414344A=CA1826307105SLC39A4c.1067T= (p.Val356=)
c.992T= (p.Val331=)
c.785T= (p.Val262=)
8g.144414344A>CCA4941411SLC39A4c.1067T>G (p.Val356Gly)
c.992T>G (p.Val331Gly)
c.785T>G (p.Val262Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414344A>GCA372621236SLC39A4c.1067T>C (p.Val356Ala)
c.992T>C (p.Val331Ala)
c.785T>C (p.Val262Ala)
8g.144414344A>TCA372621235SLC39A4c.1067T>A (p.Val356Asp)
c.992T>A (p.Val331Asp)
c.785T>A (p.Val262Asp)
8g.144414344_144414345delinsACCA1826307104SLC39A4c.1066_1067delinsGT (p.Val356=)
c.991_992delinsGT (p.Val331=)
c.784_785delinsGT (p.Val262=)
8g.144414345C>ACA372621237SLC39A4c.1066G>T (p.Val356Phe)
c.991G>T (p.Val331Phe)
c.784G>T (p.Val262Phe)
 ClinVar dbSNP gnomAD v4
8g.144414345C=CA1826307106SLC39A4c.1066G= (p.Val356=)
c.991G= (p.Val331=)
c.784G= (p.Val262=)
8g.144414345C>GCA372621238SLC39A4c.1066G>C (p.Val356Leu)
c.991G>C (p.Val331Leu)
c.784G>C (p.Val262Leu)
 gnomAD v4
8g.144414345C>TCA4941413SLC39A4c.1066G>A (p.Val356Ile)
c.991G>A (p.Val331Ile)
c.784G>A (p.Val262Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414350dupCA4941412SLC39A4c.1066dup (p.Val356GlyfsTer?)
c.991dup (p.Val331GlyfsTer?)
c.784dup (p.Val262GlyfsTer?)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414350delCA586164241SLC39A4c.1066del (p.Val356SerfsTer10)
c.991del (p.Val331SerfsTer10)
c.784del (p.Val262SerfsTer10)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
8g.144414346C>ACA463449661SLC39A4c.1065G>T (p.Gly355=)
c.990G>T (p.Gly330=)
c.783G>T (p.Gly261=)
 gnomAD v4
8g.144414346C=CA1826307107SLC39A4c.1065G= (p.Gly355=)
c.990G= (p.Gly330=)
c.783G= (p.Gly261=)
8g.144414346C>GCA463449663SLC39A4c.1065G>C (p.Gly355=)
c.990G>C (p.Gly330=)
c.783G>C (p.Gly261=)
 dbSNP
8g.144414346C>TCA463449665SLC39A4c.1065G>A (p.Gly355=)
c.990G>A (p.Gly330=)
c.783G>A (p.Gly261=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
8g.144414347C>ACA187648236SLC39A4c.1064G>T (p.Gly355Val)
c.989G>T (p.Gly330Val)
c.782G>T (p.Gly261Val)
 dbSNP gnomAD v4
8g.144414347C=CA1826307108SLC39A4c.1064G= (p.Gly355=)
c.989G= (p.Gly330=)
c.782G= (p.Gly261=)
8g.144414347C>GCA372621239SLC39A4c.1064G>C (p.Gly355Ala)
c.989G>C (p.Gly330Ala)
c.782G>C (p.Gly261Ala)
 gnomAD v4
8g.144414347C>TCA372621240SLC39A4c.1064G>A (p.Gly355Glu)
c.989G>A (p.Gly330Glu)
c.782G>A (p.Gly261Glu)
 dbSNP gnomAD v2 gnomAD v4
8g.144414348C>ACA372621241SLC39A4c.1063G>T (p.Gly355Trp)
c.988G>T (p.Gly330Trp)
c.781G>T (p.Gly261Trp)
8g.144414348C=CA1826307109SLC39A4c.1063G= (p.Gly355=)
c.988G= (p.Gly330=)
c.781G= (p.Gly261=)
8g.144414348C>GCA372621243SLC39A4c.1063G>C (p.Gly355Arg)
c.988G>C (p.Gly330Arg)
c.781G>C (p.Gly261Arg)
8g.144414348C>TCA372621242SLC39A4c.1063G>A (p.Gly355Arg)
c.988G>A (p.Gly330Arg)
c.781G>A (p.Gly261Arg)
 dbSNP gnomAD v2 gnomAD v4
8g.144414349C>ACA372621244SLC39A4c.1062G>T (p.Arg354Ser)
c.987G>T (p.Arg329Ser)
c.780G>T (p.Arg260Ser)
 gnomAD v4
8g.144414349C>GCA372621245SLC39A4c.1062G>C (p.Arg354Ser)
c.987G>C (p.Arg329Ser)
c.780G>C (p.Arg260Ser)
 gnomAD v4
8g.144414349C>TCA463449666SLC39A4c.1062G>A (p.Arg354=)
c.987G>A (p.Arg329=)
c.780G>A (p.Arg260=)
 ClinVar
8g.144414350C>ACA372621246SLC39A4c.1061G>T (p.Arg354Met)
c.986G>T (p.Arg329Met)
c.779G>T (p.Arg260Met)
 gnomAD v4
8g.144414350C=CA1826307110SLC39A4c.1061G= (p.Arg354=)
c.986G= (p.Arg329=)
c.779G= (p.Arg260=)
8g.144414350C>GCA372621247SLC39A4c.1061G>C (p.Arg354Thr)
c.986G>C (p.Arg329Thr)
c.779G>C (p.Arg260Thr)
 gnomAD v4
8g.144414350C>TCA4941414SLC39A4c.1061G>A (p.Arg354Lys)
c.986G>A (p.Arg329Lys)
c.779G>A (p.Arg260Lys)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414351T>ACA372621248SLC39A4c.1060A>T (p.Arg354Trp)
c.985A>T (p.Arg329Trp)
c.778A>T (p.Arg260Trp)
8g.144414351T>CCA372621249SLC39A4c.1060A>G (p.Arg354Gly)
c.985A>G (p.Arg329Gly)
c.778A>G (p.Arg260Gly)
8g.144414351T>GCA463449668SLC39A4c.1060A>C (p.Arg354=)
c.985A>C (p.Arg329=)
c.778A>C (p.Arg260=)
 gnomAD v4
8g.144414352G>ACA463449669SLC39A4c.1059C>T (p.Cys353=)
c.984C>T (p.Cys328=)
c.777C>T (p.Cys259=)
 gnomAD v4
8g.144414352G>CCA372621250SLC39A4c.1059C>G (p.Cys353Trp)
c.984C>G (p.Cys328Trp)
c.777C>G (p.Cys259Trp)
 ClinVar dbSNP
8g.144414352G=CA1826307111SLC39A4c.1059C= (p.Cys353=)
c.984C= (p.Cys328=)
c.777C= (p.Cys259=)
8g.144414352G>TCA372621251SLC39A4c.1059C>A (p.Cys353Ter)
c.984C>A (p.Cys328Ter)
c.777C>A (p.Cys259Ter)
 gnomAD v4
8g.144414353C>ACA372621252SLC39A4c.1058G>T (p.Cys353Phe)
c.983G>T (p.Cys328Phe)
c.776G>T (p.Cys259Phe)
 gnomAD v4
8g.144414353C>GCA372621253SLC39A4c.1058G>C (p.Cys353Ser)
c.983G>C (p.Cys328Ser)
c.776G>C (p.Cys259Ser)
8g.144414353C>TCA372621254SLC39A4c.1058G>A (p.Cys353Tyr)
c.983G>A (p.Cys328Tyr)
c.776G>A (p.Cys259Tyr)
8g.144414354A=CA1826307112SLC39A4c.1057T= (p.Cys353=)
c.982T= (p.Cys328=)
c.775T= (p.Cys259=)
8g.144414354A>CCA372621257SLC39A4c.1057T>G (p.Cys353Gly)
c.982T>G (p.Cys328Gly)
c.775T>G (p.Cys259Gly)
8g.144414354A>GCA372621255SLC39A4c.1057T>C (p.Cys353Arg)
c.982T>C (p.Cys328Arg)
c.775T>C (p.Cys259Arg)
 dbSNP gnomAD v4
8g.144414354A>TCA372621256SLC39A4c.1057T>A (p.Cys353Ser)
c.982T>A (p.Cys328Ser)
c.775T>A (p.Cys259Ser)
8g.144414356_144414378delCA2689098813SLC39A4c.1035_1057del (p.Leu346GlnfsTer?)
c.960_982del (p.Leu321GlnfsTer?)
c.753_775del (p.Leu252GlnfsTer?)
 gnomAD v4
8g.144414355G>ACA4941415SLC39A4c.1056C>T (p.Gly352=)
c.981C>T (p.Gly327=)
c.774C>T (p.Gly258=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414355G>CCA463449670SLC39A4c.1056C>G (p.Gly352=)
c.981C>G (p.Gly327=)
c.774C>G (p.Gly258=)
8g.144414355G=CA1826307113SLC39A4c.1056C= (p.Gly352=)
c.981C= (p.Gly327=)
c.774C= (p.Gly258=)
8g.144414355G>TCA463449672SLC39A4c.1056C>A (p.Gly352=)
c.981C>A (p.Gly327=)
c.774C>A (p.Gly258=)
 gnomAD v4
8g.144414356C>ACA372621258SLC39A4c.1055G>T (p.Gly352Val)
c.980G>T (p.Gly327Val)
c.773G>T (p.Gly258Val)
8g.144414356C>GCA372621259SLC39A4c.1055G>C (p.Gly352Ala)
c.980G>C (p.Gly327Ala)
c.773G>C (p.Gly258Ala)
8g.144414356C>TCA372621260SLC39A4c.1055G>A (p.Gly352Asp)
c.980G>A (p.Gly327Asp)
c.773G>A (p.Gly258Asp)
 gnomAD v4
8g.144414357C>ACA372621261SLC39A4c.1054G>T (p.Gly352Cys)
c.979G>T (p.Gly327Cys)
c.772G>T (p.Gly258Cys)
 gnomAD v4
8g.144414357C=CA1826307114SLC39A4c.1054G= (p.Gly352=)
c.979G= (p.Gly327=)
c.772G= (p.Gly258=)
8g.144414357C>GCA372621262SLC39A4c.1054G>C (p.Gly352Arg)
c.979G>C (p.Gly327Arg)
c.772G>C (p.Gly258Arg)
8g.144414357C>TCA372621263SLC39A4c.1054G>A (p.Gly352Ser)
c.979G>A (p.Gly327Ser)
c.772G>A (p.Gly258Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414358A=CA1826307115SLC39A4c.1053T= (p.Thr351=)
c.978T= (p.Thr326=)
c.771T= (p.Thr257=)
8g.144414358A>CCA463449673SLC39A4c.1053T>G (p.Thr351=)
c.978T>G (p.Thr326=)
c.771T>G (p.Thr257=)
8g.144414358A>GCA463449674SLC39A4c.1053T>C (p.Thr351=)
c.978T>C (p.Thr326=)
c.771T>C (p.Thr257=)
 dbSNP
8g.144414358A>TCA463449675SLC39A4c.1053T>A (p.Thr351=)
c.978T>A (p.Thr326=)
c.771T>A (p.Thr257=)
8g.144414359G>ACA372621264SLC39A4c.1052C>T (p.Thr351Ile)
c.977C>T (p.Thr326Ile)
c.770C>T (p.Thr257Ile)
 gnomAD v4
8g.144414359G>CCA372621265SLC39A4c.1052C>G (p.Thr351Ser)
c.977C>G (p.Thr326Ser)
c.770C>G (p.Thr257Ser)
 gnomAD v4
8g.144414359G>TCA372621266SLC39A4c.1052C>A (p.Thr351Asn)
c.977C>A (p.Thr326Asn)
c.770C>A (p.Thr257Asn)
8g.144414360T>ACA372621268SLC39A4c.1051A>T (p.Thr351Ser)
c.976A>T (p.Thr326Ser)
c.769A>T (p.Thr257Ser)
8g.144414360T>CCA4941416SLC39A4c.1051A>G (p.Thr351Ala)
c.976A>G (p.Thr326Ala)
c.769A>G (p.Thr257Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414360T>GCA372621267SLC39A4c.1051A>C (p.Thr351Pro)
c.976A>C (p.Thr326Pro)
c.769A>C (p.Thr257Pro)
8g.144414360T=CA1826307116SLC39A4c.1051A= (p.Thr351=)
c.976A= (p.Thr326=)
c.769A= (p.Thr257=)
8g.144414361G>ACA463449678SLC39A4c.1050C>T (p.Cys350=)
c.975C>T (p.Cys325=)
c.768C>T (p.Cys256=)
 gnomAD v4
8g.144414361G>CCA372621269SLC39A4c.1050C>G (p.Cys350Trp)
c.975C>G (p.Cys325Trp)
c.768C>G (p.Cys256Trp)
8g.144414361G>TCA372621270SLC39A4c.1050C>A (p.Cys350Ter)
c.975C>A (p.Cys325Ter)
c.768C>A (p.Cys256Ter)
 gnomAD v4
8g.144414362C>ACA372621271SLC39A4c.1049G>T (p.Cys350Phe)
c.974G>T (p.Cys325Phe)
c.767G>T (p.Cys256Phe)
 dbSNP
8g.144414362C=CA1826307117SLC39A4c.1049G= (p.Cys350=)
c.974G= (p.Cys325=)
c.767G= (p.Cys256=)
8g.144414362C>GCA372621272SLC39A4c.1049G>C (p.Cys350Ser)
c.974G>C (p.Cys325Ser)
c.767G>C (p.Cys256Ser)
 dbSNP gnomAD v4
8g.144414362C>TCA372621273SLC39A4c.1049G>A (p.Cys350Tyr)
c.974G>A (p.Cys325Tyr)
c.767G>A (p.Cys256Tyr)
 dbSNP gnomAD v4
8g.144414363A>CCA372621274SLC39A4c.1048T>G (p.Cys350Gly)
c.973T>G (p.Cys325Gly)
c.766T>G (p.Cys256Gly)
8g.144414363A>GCA372621275SLC39A4c.1048T>C (p.Cys350Arg)
c.973T>C (p.Cys325Arg)
c.766T>C (p.Cys256Arg)
 gnomAD v4
8g.144414363A>TCA372621276SLC39A4c.1048T>A (p.Cys350Ser)
c.973T>A (p.Cys325Ser)
c.766T>A (p.Cys256Ser)
8g.144414364G>ACA463449681SLC39A4c.1047C>T (p.Thr349=)
c.972C>T (p.Thr324=)
c.765C>T (p.Thr255=)
 gnomAD v4
8g.144414364G>CCA463449684SLC39A4c.1047C>G (p.Thr349=)
c.972C>G (p.Thr324=)
c.765C>G (p.Thr255=)
 dbSNP gnomAD v3 gnomAD v4
8g.144414364G=CA1826307118SLC39A4c.1047C= (p.Thr349=)
c.972C= (p.Thr324=)
c.765C= (p.Thr255=)
8g.144414364G>TCA463449682SLC39A4c.1047C>A (p.Thr349=)
c.972C>A (p.Thr324=)
c.765C>A (p.Thr255=)
 gnomAD v4
8g.144414364_144414370dupCA2689098887SLC39A4c.1041_1047dup (p.Cys350AlafsTer?)
c.966_972dup (p.Cys325AlafsTer?)
c.759_765dup (p.Cys256AlafsTer?)
 gnomAD v4
8g.144414365G>ACA372621277SLC39A4c.1046C>T (p.Thr349Ile)
c.971C>T (p.Thr324Ile)
c.764C>T (p.Thr255Ile)
 gnomAD v4
8g.144414365G>CCA372621278SLC39A4c.1046C>G (p.Thr349Ser)
c.971C>G (p.Thr324Ser)
c.764C>G (p.Thr255Ser)
8g.144414365G=CA1826307119SLC39A4c.1046C= (p.Thr349=)
c.971C= (p.Thr324=)
c.764C= (p.Thr255=)
8g.144414365G>TCA372621279SLC39A4c.1046C>A (p.Thr349Asn)
c.971C>A (p.Thr324Asn)
c.764C>A (p.Thr255Asn)
 dbSNP gnomAD v2 gnomAD v4
8g.144414366T>ACA372621280SLC39A4c.1045A>T (p.Thr349Ser)
c.970A>T (p.Thr324Ser)
c.763A>T (p.Thr255Ser)
8g.144414366T>CCA372621281SLC39A4c.1045A>G (p.Thr349Ala)
c.970A>G (p.Thr324Ala)
c.763A>G (p.Thr255Ala)
 gnomAD v4
8g.144414366T>GCA372621282SLC39A4c.1045A>C (p.Thr349Pro)
c.970A>C (p.Thr324Pro)
c.763A>C (p.Thr255Pro)
 dbSNP
8g.144414366T=CA1826307120SLC39A4c.1045A= (p.Thr349=)
c.970A= (p.Thr324=)
c.763A= (p.Thr255=)
8g.144414367C>ACA463449686SLC39A4c.1044G>T (p.Leu348=)
c.969G>T (p.Leu323=)
c.762G>T (p.Leu254=)
8g.144414367C=CA1826307121SLC39A4c.1044G= (p.Leu348=)
c.969G= (p.Leu323=)
c.762G= (p.Leu254=)
8g.144414367C>GCA463449687SLC39A4c.1044G>C (p.Leu348=)
c.969G>C (p.Leu323=)
c.762G>C (p.Leu254=)
8g.144414367C>TCA4941417SLC39A4c.1044G>A (p.Leu348=)
c.969G>A (p.Leu323=)
c.762G>A (p.Leu254=)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414368A>CCA372621283SLC39A4c.1043T>G (p.Leu348Arg)
c.968T>G (p.Leu323Arg)
c.761T>G (p.Leu254Arg)
8g.144414368A>GCA372621284SLC39A4c.1043T>C (p.Leu348Pro)
c.968T>C (p.Leu323Pro)
c.761T>C (p.Leu254Pro)
8g.144414368A>TCA372621285SLC39A4c.1043T>A (p.Leu348Gln)
c.968T>A (p.Leu323Gln)
c.761T>A (p.Leu254Gln)
8g.144414369G>ACA463449689SLC39A4c.1042C>T (p.Leu348=)
c.967C>T (p.Leu323=)
c.760C>T (p.Leu254=)
 gnomAD v4
8g.144414369G>CCA372621286SLC39A4c.1042C>G (p.Leu348Val)
c.967C>G (p.Leu323Val)
c.760C>G (p.Leu254Val)
8g.144414369G>TCA372621287SLC39A4c.1042C>A (p.Leu348Met)
c.967C>A (p.Leu323Met)
c.760C>A (p.Leu254Met)
8g.144414370C>ACA463449690SLC39A4c.1041G>T (p.Leu347=)
c.966G>T (p.Leu322=)
c.759G>T (p.Leu253=)
 gnomAD v4
8g.144414370C>GCA463449691SLC39A4c.1041G>C (p.Leu347=)
c.966G>C (p.Leu322=)
c.759G>C (p.Leu253=)
8g.144414370C>TCA463449692SLC39A4c.1041G>A (p.Leu347=)
c.966G>A (p.Leu322=)
c.759G>A (p.Leu253=)
8g.144414371A>CCA372621288SLC39A4c.1040T>G (p.Leu347Arg)
c.965T>G (p.Leu322Arg)
c.758T>G (p.Leu253Arg)
8g.144414371A>GCA372621289SLC39A4c.1040T>C (p.Leu347Pro)
c.965T>C (p.Leu322Pro)
c.758T>C (p.Leu253Pro)
8g.144414371A>TCA372621290SLC39A4c.1040T>A (p.Leu347Gln)
c.965T>A (p.Leu322Gln)
c.758T>A (p.Leu253Gln)
8g.144414372G>ACA463449693SLC39A4c.1039C>T (p.Leu347=)
c.964C>T (p.Leu322=)
c.757C>T (p.Leu253=)
 dbSNP gnomAD v2 gnomAD v4
8g.144414372G>CCA372621291SLC39A4c.1039C>G (p.Leu347Val)
c.964C>G (p.Leu322Val)
c.757C>G (p.Leu253Val)
8g.144414372G=CA1826307122SLC39A4c.1039C= (p.Leu347=)
c.964C= (p.Leu322=)
c.757C= (p.Leu253=)
8g.144414372G>TCA372621292SLC39A4c.1039C>A (p.Leu347Met)
c.964C>A (p.Leu322Met)
c.757C>A (p.Leu253Met)
 gnomAD v4
8g.144414373C>ACA463449695SLC39A4c.1038G>T (p.Leu346=)
c.963G>T (p.Leu321=)
c.756G>T (p.Leu252=)
 gnomAD v4
8g.144414373C>GCA463449696SLC39A4c.1038G>C (p.Leu346=)
c.963G>C (p.Leu321=)
c.756G>C (p.Leu252=)
8g.144414373C>TCA463449697SLC39A4c.1038G>A (p.Leu346=)
c.963G>A (p.Leu321=)
c.756G>A (p.Leu252=)
 ClinVar dbSNP
8g.144414374A>CCA372621293SLC39A4c.1037T>G (p.Leu346Arg)
c.962T>G (p.Leu321Arg)
c.755T>G (p.Leu252Arg)
8g.144414374A>GCA372621294SLC39A4c.1037T>C (p.Leu346Pro)
c.962T>C (p.Leu321Pro)
c.755T>C (p.Leu252Pro)
8g.144414374A>TCA372621295SLC39A4c.1037T>A (p.Leu346Gln)
c.962T>A (p.Leu321Gln)
c.755T>A (p.Leu252Gln)
8g.144414375G>ACA463449698SLC39A4c.1036C>T (p.Leu346=)
c.961C>T (p.Leu321=)
c.754C>T (p.Leu252=)
 gnomAD v4
8g.144414375G>CCA372621296SLC39A4c.1036C>G (p.Leu346Val)
c.961C>G (p.Leu321Val)
c.754C>G (p.Leu252Val)
8g.144414375G=CA1826307123SLC39A4c.1036C= (p.Leu346=)
c.961C= (p.Leu321=)
c.754C= (p.Leu252=)
8g.144414375G>TCA372621297SLC39A4c.1036C>A (p.Leu346Met)
c.961C>A (p.Leu321Met)
c.754C>A (p.Leu252Met)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414376G>ACA463449699SLC39A4c.1035C>T (p.Leu345=)
c.960C>T (p.Leu320=)
c.753C>T (p.Leu251=)
 dbSNP gnomAD v2 gnomAD v4
8g.144414376G>CCA463449700SLC39A4c.1035C>G (p.Leu345=)
c.960C>G (p.Leu320=)
c.753C>G (p.Leu251=)
 ClinVar dbSNP gnomAD v4
8g.144414376G=CA1826307124SLC39A4c.1035C= (p.Leu345=)
c.960C= (p.Leu320=)
c.753C= (p.Leu251=)
8g.144414376G>TCA4941418SLC39A4c.1035C>A (p.Leu345=)
c.960C>A (p.Leu320=)
c.753C>A (p.Leu251=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414377A>CCA372621298SLC39A4c.1034T>G (p.Leu345Arg)
c.959T>G (p.Leu320Arg)
c.752T>G (p.Leu251Arg)
8g.144414377A>GCA372621299SLC39A4c.1034T>C (p.Leu345Pro)
c.959T>C (p.Leu320Pro)
c.752T>C (p.Leu251Pro)
 gnomAD v4
8g.144414377A>TCA372621300SLC39A4c.1034T>A (p.Leu345His)
c.959T>A (p.Leu320His)
c.752T>A (p.Leu251His)
8g.144414378G>ACA372621301SLC39A4c.1033C>T (p.Leu345Phe)
c.958C>T (p.Leu320Phe)
c.751C>T (p.Leu251Phe)
 dbSNP gnomAD v2 gnomAD v4
8g.144414378G>CCA372621302SLC39A4c.1033C>G (p.Leu345Val)
c.958C>G (p.Leu320Val)
c.751C>G (p.Leu251Val)
8g.144414378G=CA1826307125SLC39A4c.1033C= (p.Leu345=)
c.958C= (p.Leu320=)
c.751C= (p.Leu251=)
8g.144414378G>TCA372621303SLC39A4c.1033C>A (p.Leu345Ile)
c.958C>A (p.Leu320Ile)
c.751C>A (p.Leu251Ile)
 gnomAD v4
8g.144414379dupCA2689098921SLC39A4c.1033dup (p.Leu345ProfsTer?)
c.958dup (p.Leu320ProfsTer?)
c.751dup (p.Leu251ProfsTer?)
 gnomAD v4
8g.144414379G>ACA463449701SLC39A4c.1032C>T (p.Gly344=)
c.957C>T (p.Gly319=)
c.750C>T (p.Gly250=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414379G>CCA463449702SLC39A4c.1032C>G (p.Gly344=)
c.957C>G (p.Gly319=)
c.750C>G (p.Gly250=)
8g.144414379G=CA1826307126SLC39A4c.1032C= (p.Gly344=)
c.957C= (p.Gly319=)
c.750C= (p.Gly250=)
8g.144414379G>TCA463449703SLC39A4c.1032C>A (p.Gly344=)
c.957C>A (p.Gly319=)
c.750C>A (p.Gly250=)
 ClinVar dbSNP gnomAD v4
8g.144414380C>ACA372621305SLC39A4c.1031G>T (p.Gly344Val)
c.956G>T (p.Gly319Val)
c.749G>T (p.Gly250Val)
8g.144414380C=CA1826307127SLC39A4c.1031G= (p.Gly344=)
c.956G= (p.Gly319=)
c.749G= (p.Gly250=)
8g.144414380C>GCA372621304SLC39A4c.1031G>C (p.Gly344Ala)
c.956G>C (p.Gly319Ala)
c.749G>C (p.Gly250Ala)
8g.144414380C>TCA4941419SLC39A4c.1031G>A (p.Gly344Asp)
c.956G>A (p.Gly319Asp)
c.749G>A (p.Gly250Asp)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414381C>ACA372621306SLC39A4c.1030G>T (p.Gly344Cys)
c.955G>T (p.Gly319Cys)
c.748G>T (p.Gly250Cys)
8g.144414381C=CA1826307128SLC39A4c.1030G= (p.Gly344=)
c.955G= (p.Gly319=)
c.748G= (p.Gly250=)
8g.144414381C>GCA372621307SLC39A4c.1030G>C (p.Gly344Arg)
c.955G>C (p.Gly319Arg)
c.748G>C (p.Gly250Arg)
8g.144414381C>TCA372621308SLC39A4c.1030G>A (p.Gly344Ser)
c.955G>A (p.Gly319Ser)
c.748G>A (p.Gly250Ser)
 dbSNP gnomAD v2 gnomAD v4
8g.144414382A>CCA372621309SLC39A4c.1029T>G (p.Phe343Leu)
c.954T>G (p.Phe318Leu)
c.747T>G (p.Phe249Leu)
8g.144414382A>GCA463449705SLC39A4c.1029T>C (p.Phe343=)
c.954T>C (p.Phe318=)
c.747T>C (p.Phe249=)
8g.144414382A>TCA372621310SLC39A4c.1029T>A (p.Phe343Leu)
c.954T>A (p.Phe318Leu)
c.747T>A (p.Phe249Leu)
8g.144414383A=CA1826307129SLC39A4c.1028T= (p.Phe343=)
c.953T= (p.Phe318=)
c.746T= (p.Phe249=)
8g.144414383A>CCA372621311SLC39A4c.1028T>G (p.Phe343Cys)
c.953T>G (p.Phe318Cys)
c.746T>G (p.Phe249Cys)
8g.144414383A>GCA372621313SLC39A4c.1028T>C (p.Phe343Ser)
c.953T>C (p.Phe318Ser)
c.746T>C (p.Phe249Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414383A>TCA372621312SLC39A4c.1028T>A (p.Phe343Tyr)
c.953T>A (p.Phe318Tyr)
c.746T>A (p.Phe249Tyr)
8g.144414384A>CCA372621314SLC39A4c.1027T>G (p.Phe343Val)
c.952T>G (p.Phe318Val)
c.745T>G (p.Phe249Val)
8g.144414384A>GCA372621315SLC39A4c.1027T>C (p.Phe343Leu)
c.952T>C (p.Phe318Leu)
c.745T>C (p.Phe249Leu)
8g.144414384A>TCA372621316SLC39A4c.1027T>A (p.Phe343Ile)
c.952T>A (p.Phe318Ile)
c.745T>A (p.Phe249Ile)
8g.144414385G>ACA463449707SLC39A4c.1026C>T (p.Val342=)
c.951C>T (p.Val317=)
c.744C>T (p.Val248=)
 gnomAD v4
8g.144414385G>CCA463449708SLC39A4c.1026C>G (p.Val342=)
c.951C>G (p.Val317=)
c.744C>G (p.Val248=)
 gnomAD v4
8g.144414385G>TCA463449709SLC39A4c.1026C>A (p.Val342=)
c.951C>A (p.Val317=)
c.744C>A (p.Val248=)
 gnomAD v4
8g.144414386A=CA1826307130SLC39A4c.1025T= (p.Val342=)
c.950T= (p.Val317=)
c.743T= (p.Val248=)
8g.144414386A>CCA372621317SLC39A4c.1025T>G (p.Val342Gly)
c.950T>G (p.Val317Gly)
c.743T>G (p.Val248Gly)
8g.144414386A>GCA372621318SLC39A4c.1025T>C (p.Val342Ala)
c.950T>C (p.Val317Ala)
c.743T>C (p.Val248Ala)
 dbSNP gnomAD v3 gnomAD v4
8g.144414386A>TCA372621319SLC39A4c.1025T>A (p.Val342Asp)
c.950T>A (p.Val317Asp)
c.743T>A (p.Val248Asp)
8g.144414387C>ACA372621320SLC39A4c.1024G>T (p.Val342Phe)
c.949G>T (p.Val317Phe)
c.742G>T (p.Val248Phe)
 gnomAD v4
8g.144414387C>GCA372621321SLC39A4c.1024G>C (p.Val342Leu)
c.949G>C (p.Val317Leu)
c.742G>C (p.Val248Leu)
8g.144414387C>TCA372621322SLC39A4c.1024G>A (p.Val342Ile)
c.949G>A (p.Val317Ile)
c.742G>A (p.Val248Ile)
8g.144414388C>ACA463449710SLC39A4c.1023G>T (p.Ala341=)
c.948G>T (p.Ala316=)
c.741G>T (p.Ala247=)
8g.144414388C=CA1826307131SLC39A4c.1023G= (p.Ala341=)
c.948G= (p.Ala316=)
c.741G= (p.Ala247=)
8g.144414388C>GCA4941421SLC39A4c.1023G>C (p.Ala341=)
c.948G>C (p.Ala316=)
c.741G>C (p.Ala247=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414388C>TCA4941420SLC39A4c.1023G>A (p.Ala341=)
c.948G>A (p.Ala316=)
c.741G>A (p.Ala247=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414389G>ACA4941422SLC39A4c.1022C>T (p.Ala341Val)
c.947C>T (p.Ala316Val)
c.740C>T (p.Ala247Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414389G>CCA372621324SLC39A4c.1022C>G (p.Ala341Gly)
c.947C>G (p.Ala316Gly)
c.740C>G (p.Ala247Gly)
8g.144414389G=CA1826307132SLC39A4c.1022C= (p.Ala341=)
c.947C= (p.Ala316=)
c.740C= (p.Ala247=)
8g.144414389G>TCA372621323SLC39A4c.1022C>A (p.Ala341Glu)
c.947C>A (p.Ala316Glu)
c.740C>A (p.Ala247Glu)
 gnomAD v4
8g.144414390C>ACA372621325SLC39A4c.1021G>T (p.Ala341Ser)
c.946G>T (p.Ala316Ser)
c.739G>T (p.Ala247Ser)
 ClinVar gnomAD v4
8g.144414390C=CA1826307133SLC39A4c.1021G= (p.Ala341=)
c.946G= (p.Ala316=)
c.739G= (p.Ala247=)
8g.144414390C>GCA372621326SLC39A4c.1021G>C (p.Ala341Pro)
c.946G>C (p.Ala316Pro)
c.739G>C (p.Ala247Pro)
8g.144414390C>TCA4941423SLC39A4c.1021G>A (p.Ala341Thr)
c.946G>A (p.Ala316Thr)
c.739G>A (p.Ala247Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414391G>ACA4941424SLC39A4c.1020C>T (p.Cys340=)
c.945C>T (p.Cys315=)
c.738C>T (p.Cys246=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414391G>CCA372621327SLC39A4c.1020C>G (p.Cys340Trp)
c.945C>G (p.Cys315Trp)
c.738C>G (p.Cys246Trp)
 gnomAD v4
8g.144414391G=CA1826307135SLC39A4c.1020C= (p.Cys340=)
c.945C= (p.Cys315=)
c.738C= (p.Cys246=)
8g.144414391G>TCA372621328SLC39A4c.1020C>A (p.Cys340Ter)
c.945C>A (p.Cys315Ter)
c.738C>A (p.Cys246Ter)
 dbSNP gnomAD v4
8g.144414392_144414400dupCA1826307134SLC39A4c.1012_1020dup (p.Cys340_Ala341insCysLeuCys)
c.937_945dup (p.Cys315_Ala316insCysLeuCys)
c.730_738dup (p.Cys246_Ala247insCysLeuCys)
 dbSNP
8g.144414393_144414409dupCA915947392SLC39A4c.1004_1020dup (p.Ala341CysfsTer14)
c.929_945dup (p.Ala316CysfsTer14)
c.722_738dup (p.Ala247CysfsTer14)
 ClinVar dbSNP

Number of alleles fetched