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.144413980_144414021dupCA586163377SLC39A4c.1225_1266dup (p.Leu422_Leu423insGlyLeuTyrAlaPhePheLeuPheGluAsnLeuPheAsnLeu)
c.1150_1191dup (p.Leu397_Leu398insGlyLeuTyrAlaPhePheLeuPheGluAsnLeuPheAsnLeu)
n.62_103dup
c.943_984dup (p.Leu328_Leu329insGlyLeuTyrAlaPhePheLeuPheGluAsnLeuPheAsnLeu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144413991G>ACA4941317SLC39A4c.1254C>T (p.Asn418=)
c.1179C>T (p.Asn393=)
n.91C>T
c.972C>T (p.Asn324=)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144413991G>CCA372619677SLC39A4c.1254C>G (p.Asn418Lys)
c.1179C>G (p.Asn393Lys)
n.91C>G
c.972C>G (p.Asn324Lys)
8g.144413991G=CA1826306874SLC39A4c.1254C= (p.Asn418=)
c.1179C= (p.Asn393=)
n.91C=
c.972C= (p.Asn324=)
8g.144413991G>TCA372619679SLC39A4c.1254C>A (p.Asn418Lys)
c.1179C>A (p.Asn393Lys)
n.91C>A
c.972C>A (p.Asn324Lys)
 gnomAD v4
8g.144413992T>ACA372619683SLC39A4c.1253A>T (p.Asn418Ile)
c.1178A>T (p.Asn393Ile)
n.90A>T
c.971A>T (p.Asn324Ile)
8g.144413992T>CCA372619684SLC39A4c.1253A>G (p.Asn418Ser)
c.1178A>G (p.Asn393Ser)
n.90A>G
c.971A>G (p.Asn324Ser)
8g.144413992T>GCA372619686SLC39A4c.1253A>C (p.Asn418Thr)
c.1178A>C (p.Asn393Thr)
n.90A>C
c.971A>C (p.Asn324Thr)
8g.144413993T>ACA372619694SLC39A4c.1252A>T (p.Asn418Tyr)
c.1177A>T (p.Asn393Tyr)
n.89A>T
c.970A>T (p.Asn324Tyr)
8g.144413993T>CCA372619691SLC39A4c.1252A>G (p.Asn418Asp)
c.1177A>G (p.Asn393Asp)
n.89A>G
c.970A>G (p.Asn324Asp)
8g.144413993T>GCA372619689SLC39A4c.1252A>C (p.Asn418His)
c.1177A>C (p.Asn393His)
n.89A>C
c.970A>C (p.Asn324His)
8g.144413994C>ACA372619697SLC39A4c.1251G>T (p.Glu417Asp)
c.1176G>T (p.Glu392Asp)
n.88G>T
c.969G>T (p.Glu323Asp)
8g.144413994C=CA1826306875SLC39A4c.1251G= (p.Glu417=)
c.1176G= (p.Glu392=)
n.88G=
c.969G= (p.Glu323=)
8g.144413994C>GCA372619699SLC39A4c.1251G>C (p.Glu417Asp)
c.1176G>C (p.Glu392Asp)
n.88G>C
c.969G>C (p.Glu323Asp)
8g.144413994C>TCA4941318SLC39A4c.1251G>A (p.Glu417=)
c.1176G>A (p.Glu392=)
n.88G>A
c.969G>A (p.Glu323=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144413995T>ACA372619709SLC39A4c.1250A>T (p.Glu417Val)
c.1175A>T (p.Glu392Val)
n.87A>T
c.968A>T (p.Glu323Val)
8g.144413995T>CCA372619711SLC39A4c.1250A>G (p.Glu417Gly)
c.1175A>G (p.Glu392Gly)
n.87A>G
c.968A>G (p.Glu323Gly)
8g.144413995T>GCA372619712SLC39A4c.1250A>C (p.Glu417Ala)
c.1175A>C (p.Glu392Ala)
n.87A>C
c.968A>C (p.Glu323Ala)
8g.144413996C>ACA372619716SLC39A4c.1249G>T (p.Glu417Ter)
c.1174G>T (p.Glu392Ter)
n.86G>T
c.967G>T (p.Glu323Ter)
 gnomAD v4
8g.144413996C>GCA372619718SLC39A4c.1249G>C (p.Glu417Gln)
c.1174G>C (p.Glu392Gln)
n.86G>C
c.967G>C (p.Glu323Gln)
8g.144413996C>TCA372619721SLC39A4c.1249G>A (p.Glu417Lys)
c.1174G>A (p.Glu392Lys)
n.86G>A
c.967G>A (p.Glu323Lys)
 gnomAD v4
8g.144413996_144413997insTCA2580078703SLC39A4c.1248_1249insA (p.Glu417ArgfsTer26)
c.1173_1174insA (p.Glu392ArgfsTer26)
n.85_86insA
c.966_967insA (p.Glu323ArgfsTer26)
 ClinVar
8g.144413997A=CA1826306876SLC39A4c.1248T= (p.Phe416=)
c.1173T= (p.Phe391=)
n.85T=
c.966T= (p.Phe322=)
8g.144413997A>CCA372619725SLC39A4c.1248T>G (p.Phe416Leu)
c.1173T>G (p.Phe391Leu)
n.85T>G
c.966T>G (p.Phe322Leu)
8g.144413997A>GCA463556086SLC39A4c.1248T>C (p.Phe416=)
c.1173T>C (p.Phe391=)
n.85T>C
c.966T>C (p.Phe322=)
 dbSNP
8g.144413997A>TCA372619727SLC39A4c.1248T>A (p.Phe416Leu)
c.1173T>A (p.Phe391Leu)
n.85T>A
c.966T>A (p.Phe322Leu)
8g.144413998A=CA1826306877SLC39A4c.1247T= (p.Phe416=)
c.1172T= (p.Phe391=)
n.84T=
c.965T= (p.Phe322=)
8g.144413998A>CCA372619730SLC39A4c.1247T>G (p.Phe416Cys)
c.1172T>G (p.Phe391Cys)
n.84T>G
c.965T>G (p.Phe322Cys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144413998A>GCA372619732SLC39A4c.1247T>C (p.Phe416Ser)
c.1172T>C (p.Phe391Ser)
n.84T>C
c.965T>C (p.Phe322Ser)
 gnomAD v4
8g.144413998A>TCA372619734SLC39A4c.1247T>A (p.Phe416Tyr)
c.1172T>A (p.Phe391Tyr)
n.84T>A
c.965T>A (p.Phe322Tyr)
 gnomAD v4
8g.144413999A>CCA372619740SLC39A4c.1246T>G (p.Phe416Val)
c.1171T>G (p.Phe391Val)
n.83T>G
c.964T>G (p.Phe322Val)
8g.144413999A>GCA372619742SLC39A4c.1246T>C (p.Phe416Leu)
c.1171T>C (p.Phe391Leu)
n.83T>C
c.964T>C (p.Phe322Leu)
8g.144413999A>TCA372619737SLC39A4c.1246T>A (p.Phe416Ile)
c.1171T>A (p.Phe391Ile)
n.83T>A
c.964T>A (p.Phe322Ile)
8g.144414000C>ACA463556091SLC39A4c.1245G>T (p.Leu415=)
c.1170G>T (p.Leu390=)
n.82G>T
c.963G>T (p.Leu321=)
 ClinVar dbSNP
8g.144414000C>GCA463556089SLC39A4c.1245G>C (p.Leu415=)
c.1170G>C (p.Leu390=)
n.82G>C
c.963G>C (p.Leu321=)
8g.144414000C>TCA463556090SLC39A4c.1245G>A (p.Leu415=)
c.1170G>A (p.Leu390=)
n.82G>A
c.963G>A (p.Leu321=)
 ClinVar gnomAD v4
8g.144414001A>CCA372619746SLC39A4c.1244T>G (p.Leu415Arg)
c.1169T>G (p.Leu390Arg)
n.81T>G
c.962T>G (p.Leu321Arg)
8g.144414001A>GCA372619748SLC39A4c.1244T>C (p.Leu415Pro)
c.1169T>C (p.Leu390Pro)
n.81T>C
c.962T>C (p.Leu321Pro)
 gnomAD v4
8g.144414001A>TCA372619750SLC39A4c.1244T>A (p.Leu415Gln)
c.1169T>A (p.Leu390Gln)
n.81T>A
c.962T>A (p.Leu321Gln)
8g.144414002G>ACA463556094SLC39A4c.1243C>T (p.Leu415=)
c.1168C>T (p.Leu390=)
n.80C>T
c.961C>T (p.Leu321=)
8g.144414002G>CCA372619752SLC39A4c.1243C>G (p.Leu415Val)
c.1168C>G (p.Leu390Val)
n.80C>G
c.961C>G (p.Leu321Val)
8g.144414002G>TCA372619754SLC39A4c.1243C>A (p.Leu415Met)
c.1168C>A (p.Leu390Met)
n.80C>A
c.961C>A (p.Leu321Met)
 gnomAD v4
8g.144414002_144414005delinsGGAACA1826306878SLC39A4c.1240_1243delinsTTCC (p.Phe414=)
c.1165_1168delinsTTCC (p.Phe389=)
n.77_80delinsTTCC
c.958_961delinsTTCC (p.Phe320=)
8g.144414003G>ACA463556096SLC39A4c.1242C>T (p.Phe414=)
c.1167C>T (p.Phe389=)
n.79C>T
c.960C>T (p.Phe320=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
8g.144414003G>CCA372619757SLC39A4c.1242C>G (p.Phe414Leu)
c.1167C>G (p.Phe389Leu)
n.79C>G
c.960C>G (p.Phe320Leu)
8g.144414003G=CA1826306880SLC39A4c.1242C= (p.Phe414=)
c.1167C= (p.Phe389=)
n.79C=
c.960C= (p.Phe320=)
8g.144414003G>TCA372619760SLC39A4c.1242C>A (p.Phe414Leu)
c.1167C>A (p.Phe389Leu)
n.79C>A
c.960C>A (p.Phe320Leu)
 gnomAD v4
8g.144414007_144414009delCA1826306879SLC39A4c.1240_1242del (p.Phe414del)
c.1165_1167del (p.Phe389del)
n.77_79del
c.958_960del (p.Phe320del)
 dbSNP
8g.144414004A>CCA372619762SLC39A4c.1241T>G (p.Phe414Cys)
c.1166T>G (p.Phe389Cys)
n.78T>G
c.959T>G (p.Phe320Cys)
8g.144414004A>GCA372619763SLC39A4c.1241T>C (p.Phe414Ser)
c.1166T>C (p.Phe389Ser)
n.78T>C
c.959T>C (p.Phe320Ser)
8g.144414004A>TCA372619766SLC39A4c.1241T>A (p.Phe414Tyr)
c.1166T>A (p.Phe389Tyr)
n.78T>A
c.959T>A (p.Phe320Tyr)
8g.144414005A=CA1826306881SLC39A4c.1240T= (p.Phe414=)
c.1165T= (p.Phe389=)
n.77T=
c.958T= (p.Phe320=)
8g.144414005A>CCA372619769SLC39A4c.1240T>G (p.Phe414Val)
c.1165T>G (p.Phe389Val)
n.77T>G
c.958T>G (p.Phe320Val)
8g.144414005A>GCA4941319SLC39A4c.1240T>C (p.Phe414Leu)
c.1165T>C (p.Phe389Leu)
n.77T>C
c.958T>C (p.Phe320Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414005A>TCA372619774SLC39A4c.1240T>A (p.Phe414Ile)
c.1165T>A (p.Phe389Ile)
n.77T>A
c.958T>A (p.Phe320Ile)
8g.144414005_144414006delinsAGCA1826306882SLC39A4c.1239_1240delinsCT (p.Phe413=)
c.1164_1165delinsCT (p.Phe388=)
n.76_77delinsCT
c.957_958delinsCT (p.Phe319=)
8g.144414006delCA1826306883SLC39A4c.1239del (p.Phe414SerfsTer?)
c.1164del (p.Phe389SerfsTer?)
n.76del
c.957del (p.Phe320SerfsTer?)
 dbSNP
8g.144414006G>ACA463556098SLC39A4c.1239C>T (p.Phe413=)
c.1164C>T (p.Phe388=)
n.76C>T
c.957C>T (p.Phe319=)
 ClinVar gnomAD v4
8g.144414006G>CCA372619777SLC39A4c.1239C>G (p.Phe413Leu)
c.1164C>G (p.Phe388Leu)
n.76C>G
c.957C>G (p.Phe319Leu)
8g.144414006G>TCA372619780SLC39A4c.1239C>A (p.Phe413Leu)
c.1164C>A (p.Phe388Leu)
n.76C>A
c.957C>A (p.Phe319Leu)
8g.144414007A=CA1826306884SLC39A4c.1238T= (p.Phe413=)
c.1163T= (p.Phe388=)
n.75T=
c.956T= (p.Phe319=)
8g.144414007A>CCA372619783SLC39A4c.1238T>G (p.Phe413Cys)
c.1163T>G (p.Phe388Cys)
n.75T>G
c.956T>G (p.Phe319Cys)
8g.144414007A>GCA372619784SLC39A4c.1238T>C (p.Phe413Ser)
c.1163T>C (p.Phe388Ser)
n.75T>C
c.956T>C (p.Phe319Ser)
8g.144414007A>TCA372619787SLC39A4c.1238T>A (p.Phe413Tyr)
c.1163T>A (p.Phe388Tyr)
n.75T>A
c.956T>A (p.Phe319Tyr)
8g.144414007_144414008insTCA1139660826SLC39A4c.1237_1238insA (p.Phe413TyrfsTer5)
c.1162_1163insA (p.Phe388TyrfsTer5)
n.74_75insA
c.955_956insA (p.Phe319TyrfsTer5)
 ClinVar dbSNP
8g.144414008A=CA1826306885SLC39A4c.1237T= (p.Phe413=)
c.1162T= (p.Phe388=)
n.74T=
c.955T= (p.Phe319=)
8g.144414008A>CCA372619790SLC39A4c.1237T>G (p.Phe413Val)
c.1162T>G (p.Phe388Val)
n.74T>G
c.955T>G (p.Phe319Val)
8g.144414008A>GCA4941320SLC39A4c.1237T>C (p.Phe413Leu)
c.1162T>C (p.Phe388Leu)
n.74T>C
c.955T>C (p.Phe319Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414008A>TCA372619793SLC39A4c.1237T>A (p.Phe413Ile)
c.1162T>A (p.Phe388Ile)
n.74T>A
c.955T>A (p.Phe319Ile)
 gnomAD v4
8g.144414009G>ACA463556102SLC39A4c.1236C>T (p.Ala412=)
c.1161C>T (p.Ala387=)
n.73C>T
c.954C>T (p.Ala318=)
 gnomAD v4
8g.144414009G>CCA463556103SLC39A4c.1236C>G (p.Ala412=)
c.1161C>G (p.Ala387=)
n.73C>G
c.954C>G (p.Ala318=)
8g.144414009G>TCA463556104SLC39A4c.1236C>A (p.Ala412=)
c.1161C>A (p.Ala387=)
n.73C>A
c.954C>A (p.Ala318=)
 gnomAD v4
8g.144414010G>ACA372619796SLC39A4c.1235C>T (p.Ala412Val)
c.1160C>T (p.Ala387Val)
n.72C>T
c.953C>T (p.Ala318Val)
 gnomAD v4
8g.144414010G>CCA372619798SLC39A4c.1235C>G (p.Ala412Gly)
c.1160C>G (p.Ala387Gly)
n.72C>G
c.953C>G (p.Ala318Gly)
8g.144414010G>TCA372619800SLC39A4c.1235C>A (p.Ala412Asp)
c.1160C>A (p.Ala387Asp)
n.72C>A
c.953C>A (p.Ala318Asp)
8g.144414011C>ACA372619805SLC39A4c.1234G>T (p.Ala412Ser)
c.1159G>T (p.Ala387Ser)
n.71G>T
c.952G>T (p.Ala318Ser)
8g.144414011C=CA1826306886SLC39A4c.1234G= (p.Ala412=)
c.1159G= (p.Ala387=)
n.71G=
c.952G= (p.Ala318=)
8g.144414011C>GCA372619807SLC39A4c.1234G>C (p.Ala412Pro)
c.1159G>C (p.Ala387Pro)
n.71G>C
c.952G>C (p.Ala318Pro)
8g.144414011C>TCA4941321SLC39A4c.1234G>A (p.Ala412Thr)
c.1159G>A (p.Ala387Thr)
n.71G>A
c.952G>A (p.Ala318Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414012G>ACA463556107SLC39A4c.1233C>T (p.Tyr411=)
c.1158C>T (p.Tyr386=)
n.70C>T
c.951C>T (p.Tyr317=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414012G>CCA372619811SLC39A4c.1233C>G (p.Tyr411Ter)
c.1158C>G (p.Tyr386Ter)
n.70C>G
c.951C>G (p.Tyr317Ter)
8g.144414012G=CA1826306887SLC39A4c.1233C= (p.Tyr411=)
c.1158C= (p.Tyr386=)
n.70C=
c.951C= (p.Tyr317=)
8g.144414012G>TCA372619813SLC39A4c.1233C>A (p.Tyr411Ter)
c.1158C>A (p.Tyr386Ter)
n.70C>A
c.951C>A (p.Tyr317Ter)
8g.144414013T>ACA372619817SLC39A4c.1232A>T (p.Tyr411Phe)
c.1157A>T (p.Tyr386Phe)
n.69A>T
c.950A>T (p.Tyr317Phe)
 dbSNP
8g.144414013T>CCA372619821SLC39A4c.1232A>G (p.Tyr411Cys)
c.1157A>G (p.Tyr386Cys)
n.69A>G
c.950A>G (p.Tyr317Cys)
8g.144414013T>GCA372619818SLC39A4c.1232A>C (p.Tyr411Ser)
c.1157A>C (p.Tyr386Ser)
n.69A>C
c.950A>C (p.Tyr317Ser)
8g.144414013T=CA1826306888SLC39A4c.1232A= (p.Tyr411=)
c.1157A= (p.Tyr386=)
n.69A=
c.950A= (p.Tyr317=)
8g.144414014A>CCA372619823SLC39A4c.1231T>G (p.Tyr411Asp)
c.1156T>G (p.Tyr386Asp)
n.68T>G
c.949T>G (p.Tyr317Asp)
8g.144414014A>GCA372619826SLC39A4c.1231T>C (p.Tyr411His)
c.1156T>C (p.Tyr386His)
n.68T>C
c.949T>C (p.Tyr317His)
 gnomAD v4
8g.144414014A>TCA372619828SLC39A4c.1231T>A (p.Tyr411Asn)
c.1156T>A (p.Tyr386Asn)
n.68T>A
c.949T>A (p.Tyr317Asn)
8g.144414015G>ACA463556112SLC39A4c.1230C>T (p.Leu410=)
c.1155C>T (p.Leu385=)
n.67C>T
c.948C>T (p.Leu316=)
8g.144414015G>CCA463556113SLC39A4c.1230C>G (p.Leu410=)
c.1155C>G (p.Leu385=)
n.67C>G
c.948C>G (p.Leu316=)
 gnomAD v4
8g.144414015G>TCA463556114SLC39A4c.1230C>A (p.Leu410=)
c.1155C>A (p.Leu385=)
n.67C>A
c.948C>A (p.Leu316=)
 gnomAD v4
8g.144414016A>CCA372619832SLC39A4c.1229T>G (p.Leu410Arg)
c.1154T>G (p.Leu385Arg)
n.66T>G
c.947T>G (p.Leu316Arg)
8g.144414016A>GCA372619835SLC39A4c.1229T>C (p.Leu410Pro)
c.1154T>C (p.Leu385Pro)
n.66T>C
c.947T>C (p.Leu316Pro)
8g.144414016A>TCA372619838SLC39A4c.1229T>A (p.Leu410His)
c.1154T>A (p.Leu385His)
n.66T>A
c.947T>A (p.Leu316His)
8g.144414017G>ACA372619840SLC39A4c.1228C>T (p.Leu410Phe)
c.1153C>T (p.Leu385Phe)
n.65C>T
c.946C>T (p.Leu316Phe)
 gnomAD v4
8g.144414017G>CCA372619843SLC39A4c.1228C>G (p.Leu410Val)
c.1153C>G (p.Leu385Val)
n.65C>G
c.946C>G (p.Leu316Val)
8g.144414017G>TCA372619845SLC39A4c.1228C>A (p.Leu410Ile)
c.1153C>A (p.Leu385Ile)
n.65C>A
c.946C>A (p.Leu316Ile)
8g.144414020_144414024delCA2580078704SLC39A4c.1224_1228del (p.Gly409LeufsTer7)
c.1149_1153del (p.Gly384LeufsTer7)
n.61_65del
c.942_946del (p.Gly315LeufsTer7)
 ClinVar dbSNP
8g.144414018C>ACA463556117SLC39A4c.1227G>T (p.Gly409=)
c.1152G>T (p.Gly384=)
n.64G>T
c.945G>T (p.Gly315=)
 ClinVar dbSNP gnomAD v4
8g.144414018C=CA1826306889SLC39A4c.1227G= (p.Gly409=)
c.1152G= (p.Gly384=)
n.64G=
c.945G= (p.Gly315=)
8g.144414018C>GCA463556116SLC39A4c.1227G>C (p.Gly409=)
c.1152G>C (p.Gly384=)
n.64G>C
c.945G>C (p.Gly315=)
 dbSNP gnomAD v2
8g.144414018C>TCA463556118SLC39A4c.1227G>A (p.Gly409=)
c.1152G>A (p.Gly384=)
n.64G>A
c.945G>A (p.Gly315=)
 gnomAD v4
8g.144414019C>ACA372619849SLC39A4c.1226G>T (p.Gly409Val)
c.1151G>T (p.Gly384Val)
n.63G>T
c.944G>T (p.Gly315Val)
 gnomAD v4
8g.144414019C=CA1826306890SLC39A4c.1226G= (p.Gly409=)
c.1151G= (p.Gly384=)
n.63G=
c.944G= (p.Gly315=)
8g.144414019C>GCA372619851SLC39A4c.1226G>C (p.Gly409Ala)
c.1151G>C (p.Gly384Ala)
n.63G>C
c.944G>C (p.Gly315Ala)
 gnomAD v4
8g.144414019C>TCA372619853SLC39A4c.1226G>A (p.Gly409Glu)
c.1151G>A (p.Gly384Glu)
n.63G>A
c.944G>A (p.Gly315Glu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
8g.144414020C>ACA372619861SLC39A4c.1225G>T (p.Gly409Trp)
c.1150G>T (p.Gly384Trp)
n.62G>T
c.943G>T (p.Gly315Trp)
 gnomAD v4
8g.144414020C=CA1826306892SLC39A4c.1225G= (p.Gly409=)
c.1150G= (p.Gly384=)
n.62G=
c.943G= (p.Gly315=)
8g.144414020C>GCA372619857SLC39A4c.1225G>C (p.Gly409Arg)
c.1150G>C (p.Gly384Arg)
n.62G>C
c.943G>C (p.Gly315Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
8g.144414020C>TCA372619859SLC39A4c.1225G>A (p.Gly409Arg)
c.1150G>A (p.Gly384Arg)
n.62G>A
c.943G>A (p.Gly315Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414020_144414021delinsCGCA1826306891SLC39A4c.1224_1225delinsCG (p.Ala408=)
c.1149_1150delinsCG (p.Ala383=)
n.61_62delinsCG
c.942_943delinsCG (p.Ala314=)
8g.144414021G>ACA4941323SLC39A4c.1224C>T (p.Ala408=)
c.1149C>T (p.Ala383=)
n.61C>T
c.942C>T (p.Ala314=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414021G>CCA463556120SLC39A4c.1224C>G (p.Ala408=)
c.1149C>G (p.Ala383=)
n.61C>G
c.942C>G (p.Ala314=)
 ClinVar
8g.144414021G=CA1826306893SLC39A4c.1224C= (p.Ala408=)
c.1149C= (p.Ala383=)
n.61C=
c.942C= (p.Ala314=)
8g.144414021G>TCA463556122SLC39A4c.1224C>A (p.Ala408=)
c.1149C>A (p.Ala383=)
n.61C>A
c.942C>A (p.Ala314=)
 ClinVar
8g.144414022delCA4941322SLC39A4c.1224del (p.Leu410SerfsTer?)
c.1149del (p.Leu385SerfsTer?)
n.61del
c.942del (p.Leu316SerfsTer?)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414022G>ACA4941324SLC39A4c.1223C>T (p.Ala408Val)
c.1148C>T (p.Ala383Val)
n.60C>T
c.941C>T (p.Ala314Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414022G>CCA372619874SLC39A4c.1223C>G (p.Ala408Gly)
c.1148C>G (p.Ala383Gly)
n.60C>G
c.941C>G (p.Ala314Gly)
8g.144414022G=CA1826306894SLC39A4c.1223C= (p.Ala408=)
c.1148C= (p.Ala383=)
n.60C=
c.941C= (p.Ala314=)
8g.144414022G>TCA372619876SLC39A4c.1223C>A (p.Ala408Asp)
c.1148C>A (p.Ala383Asp)
n.60C>A
c.941C>A (p.Ala314Asp)
8g.144414023C>ACA372619880SLC39A4c.1222G>T (p.Ala408Ser)
c.1147G>T (p.Ala383Ser)
n.59G>T
c.940G>T (p.Ala314Ser)
 gnomAD v4
8g.144414023C=CA1826306895SLC39A4c.1222G= (p.Ala408=)
c.1147G= (p.Ala383=)
n.59G=
c.940G= (p.Ala314=)
8g.144414023C>GCA187646749SLC39A4c.1222G>C (p.Ala408Pro)
c.1147G>C (p.Ala383Pro)
n.59G>C
c.940G>C (p.Ala314Pro)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414023C>TCA372619883SLC39A4c.1222G>A (p.Ala408Thr)
c.1147G>A (p.Ala383Thr)
n.59G>A
c.940G>A (p.Ala314Thr)
 ClinVar dbSNP gnomAD v4
8g.144414024C>ACA463556123SLC39A4c.1221G>T (p.Leu407=)
c.1146G>T (p.Leu382=)
n.58G>T
c.939G>T (p.Leu313=)
 gnomAD v4
8g.144414024C>GCA463556124SLC39A4c.1221G>C (p.Leu407=)
c.1146G>C (p.Leu382=)
n.58G>C
c.939G>C (p.Leu313=)
8g.144414024C>TCA463556125SLC39A4c.1221G>A (p.Leu407=)
c.1146G>A (p.Leu382=)
n.58G>A
c.939G>A (p.Leu313=)
8g.144414025A=CA1826306896SLC39A4c.1220T= (p.Leu407=)
c.1145T= (p.Leu382=)
n.57T=
c.938T= (p.Leu313=)
8g.144414025A>CCA372619885SLC39A4c.1220T>G (p.Leu407Arg)
c.1145T>G (p.Leu382Arg)
n.57T>G
c.938T>G (p.Leu313Arg)
8g.144414025A>GCA372619887SLC39A4c.1220T>C (p.Leu407Pro)
c.1145T>C (p.Leu382Pro)
n.57T>C
c.938T>C (p.Leu313Pro)
 dbSNP gnomAD v4
8g.144414025A>TCA372619889SLC39A4c.1220T>A (p.Leu407Gln)
c.1145T>A (p.Leu382Gln)
n.57T>A
c.938T>A (p.Leu313Gln)
8g.144414026G>ACA463556126SLC39A4c.1219C>T (p.Leu407=)
c.1144C>T (p.Leu382=)
n.56C>T
c.937C>T (p.Leu313=)
 dbSNP gnomAD v2 gnomAD v4
8g.144414026G>CCA372619893SLC39A4c.1219C>G (p.Leu407Val)
c.1144C>G (p.Leu382Val)
n.56C>G
c.937C>G (p.Leu313Val)
8g.144414026G=CA1826306897SLC39A4c.1219C= (p.Leu407=)
c.1144C= (p.Leu382=)
n.56C=
c.937C= (p.Leu313=)
8g.144414026G>TCA372619895SLC39A4c.1219C>A (p.Leu407Met)
c.1144C>A (p.Leu382Met)
n.56C>A
c.937C>A (p.Leu313Met)
 gnomAD v4
8g.144414027C>ACA372619898SLC39A4c.1218G>T (p.Met406Ile)
c.1143G>T (p.Met381Ile)
n.55G>T
c.936G>T (p.Met312Ile)
 gnomAD v4
8g.144414027C=CA1826306898SLC39A4c.1218G= (p.Met406=)
c.1143G= (p.Met381=)
n.55G=
c.936G= (p.Met312=)
8g.144414027C>GCA372619900SLC39A4c.1218G>C (p.Met406Ile)
c.1143G>C (p.Met381Ile)
n.55G>C
c.936G>C (p.Met312Ile)
 dbSNP gnomAD v4
8g.144414027C>TCA4941325SLC39A4c.1218G>A (p.Met406Ile)
c.1143G>A (p.Met381Ile)
n.55G>A
c.936G>A (p.Met312Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414028A>CCA372619905SLC39A4c.1217T>G (p.Met406Arg)
c.1142T>G (p.Met381Arg)
n.54T>G
c.935T>G (p.Met312Arg)
8g.144414028A>GCA372619907SLC39A4c.1217T>C (p.Met406Thr)
c.1142T>C (p.Met381Thr)
n.54T>C
c.935T>C (p.Met312Thr)
 gnomAD v4
8g.144414028A>TCA372619909SLC39A4c.1217T>A (p.Met406Lys)
c.1142T>A (p.Met381Lys)
n.54T>A
c.935T>A (p.Met312Lys)
 gnomAD v4
8g.144414028_144414029insAGAAACCCACCGCTGAGATGGCCTTGAGGTCCATCTTGCCTGACATGCCCTGGCCAATTAAGTTAGTCATTTCTTCCAACCA2782585157SLC39A4c.1216_1217insGTTGGAAGAAATGACTAACTTAATTGGCCAGGGCATGTCAGGCAAGATGGACCTCAAGGCCATCTCAGCGGTGGGTTTCT (p.Met406SerfsTer5)
c.1141_1142insGTTGGAAGAAATGACTAACTTAATTGGCCAGGGCATGTCAGGCAAGATGGACCTCAAGGCCATCTCAGCGGTGGGTTTCT (p.Met381SerfsTer5)
n.53_54insGTTGGAAGAAATGACTAACTTAATTGGCCAGGGCATGTCAGGCAAGATGGACCTCAAGGCCATCTCAGCGGTGGGTTTCT
c.934_935insGTTGGAAGAAATGACTAACTTAATTGGCCAGGGCATGTCAGGCAAGATGGACCTCAAGGCCATCTCAGCGGTGGGTTTCT (p.Met312SerfsTer5)
8g.144414029T>ACA372619912SLC39A4c.1216A>T (p.Met406Leu)
c.1141A>T (p.Met381Leu)
n.53A>T
c.934A>T (p.Met312Leu)
8g.144414029T>CCA372619914SLC39A4c.1216A>G (p.Met406Val)
c.1141A>G (p.Met381Val)
n.53A>G
c.934A>G (p.Met312Val)
8g.144414029T>GCA372619916SLC39A4c.1216A>C (p.Met406Leu)
c.1141A>C (p.Met381Leu)
n.53A>C
c.934A>C (p.Met312Leu)
8g.144414030A=CA1826306899SLC39A4c.1215T= (p.Ala405=)
c.1140T= (p.Ala380=)
n.52T=
c.933T= (p.Ala311=)
8g.144414030A>CCA463556131SLC39A4c.1215T>G (p.Ala405=)
c.1140T>G (p.Ala380=)
n.52T>G
c.933T>G (p.Ala311=)
8g.144414030A>GCA4941326SLC39A4c.1215T>C (p.Ala405=)
c.1140T>C (p.Ala380=)
n.52T>C
c.933T>C (p.Ala311=)
 dbSNP ExAC gnomAD v2
8g.144414030A>TCA463556130SLC39A4c.1215T>A (p.Ala405=)
c.1140T>A (p.Ala380=)
n.52T>A
c.933T>A (p.Ala311=)
8g.144414031G>ACA372619923SLC39A4c.1214C>T (p.Ala405Val)
c.1139C>T (p.Ala380Val)
n.51C>T
c.932C>T (p.Ala311Val)
 gnomAD v4
8g.144414031G>CCA372619925SLC39A4c.1214C>G (p.Ala405Gly)
c.1139C>G (p.Ala380Gly)
n.51C>G
c.932C>G (p.Ala311Gly)
 gnomAD v4
8g.144414031G>TCA372619926SLC39A4c.1214C>A (p.Ala405Asp)
c.1139C>A (p.Ala380Asp)
n.51C>A
c.932C>A (p.Ala311Asp)
 gnomAD v4
8g.144414032C>ACA372619933SLC39A4c.1213G>T (p.Ala405Ser)
c.1138G>T (p.Ala380Ser)
n.50G>T
c.931G>T (p.Ala311Ser)
 gnomAD v4
8g.144414032C=CA1826306900SLC39A4c.1213G= (p.Ala405=)
c.1138G= (p.Ala380=)
n.50G=
c.931G= (p.Ala311=)
8g.144414032C>GCA187646766SLC39A4c.1213G>C (p.Ala405Pro)
c.1138G>C (p.Ala380Pro)
n.50G>C
c.931G>C (p.Ala311Pro)
 dbSNP
8g.144414032C>TCA372619931SLC39A4c.1213G>A (p.Ala405Thr)
c.1138G>A (p.Ala380Thr)
n.50G>A
c.931G>A (p.Ala311Thr)
 dbSNP gnomAD v2 gnomAD v4
8g.144414033C>ACA463556133SLC39A4c.1212G>T (p.Leu404=)
c.1137G>T (p.Leu379=)
n.49G>T
c.930G>T (p.Leu310=)
 gnomAD v4
8g.144414033C=CA1826306901SLC39A4c.1212G= (p.Leu404=)
c.1137G= (p.Leu379=)
n.49G=
c.930G= (p.Leu310=)
8g.144414033C>GCA463556134SLC39A4c.1212G>C (p.Leu404=)
c.1137G>C (p.Leu379=)
n.49G>C
c.930G>C (p.Leu310=)
8g.144414033C>TCA187646769SLC39A4c.1212G>A (p.Leu404=)
c.1137G>A (p.Leu379=)
n.49G>A
c.930G>A (p.Leu310=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414034A=CA1826306902SLC39A4c.1211T= (p.Leu404=)
c.1136T= (p.Leu379=)
n.48T=
c.929T= (p.Leu310=)
8g.144414034A>CCA372619938SLC39A4c.1211T>G (p.Leu404Arg)
c.1136T>G (p.Leu379Arg)
n.48T>G
c.929T>G (p.Leu310Arg)
 dbSNP gnomAD v3 gnomAD v4
8g.144414034A>GCA372619940SLC39A4c.1211T>C (p.Leu404Pro)
c.1136T>C (p.Leu379Pro)
n.48T>C
c.929T>C (p.Leu310Pro)
 dbSNP gnomAD v4
8g.144414034A>TCA372619941SLC39A4c.1211T>A (p.Leu404Gln)
c.1136T>A (p.Leu379Gln)
n.48T>A
c.929T>A (p.Leu310Gln)
 gnomAD v4 COSMIC COSMIC
8g.144414035G>ACA463556138SLC39A4c.1210C>T (p.Leu404=)
c.1135C>T (p.Leu379=)
n.47C>T
c.928C>T (p.Leu310=)
8g.144414035G>CCA372619945SLC39A4c.1210C>G (p.Leu404Val)
c.1135C>G (p.Leu379Val)
n.47C>G
c.928C>G (p.Leu310Val)
8g.144414035G>TCA372619947SLC39A4c.1210C>A (p.Leu404Met)
c.1135C>A (p.Leu379Met)
n.47C>A
c.928C>A (p.Leu310Met)
 gnomAD v4
8g.144414036G>ACA463556141SLC39A4c.1209C>T (p.Leu403=)
c.1134C>T (p.Leu378=)
n.46C>T
c.927C>T (p.Leu309=)
 gnomAD v4
8g.144414036G>CCA463556139SLC39A4c.1209C>G (p.Leu403=)
c.1134C>G (p.Leu378=)
n.46C>G
c.927C>G (p.Leu309=)
8g.144414036G>TCA463556140SLC39A4c.1209C>A (p.Leu403=)
c.1134C>A (p.Leu378=)
n.46C>A
c.927C>A (p.Leu309=)
8g.144414037A>CCA372619950SLC39A4c.1208T>G (p.Leu403Arg)
c.1133T>G (p.Leu378Arg)
n.45T>G
c.926T>G (p.Leu309Arg)
8g.144414037A>GCA372619952SLC39A4c.1208T>C (p.Leu403Pro)
c.1133T>C (p.Leu378Pro)
n.45T>C
c.926T>C (p.Leu309Pro)
 gnomAD v4
8g.144414037A>TCA372619954SLC39A4c.1208T>A (p.Leu403His)
c.1133T>A (p.Leu378His)
n.45T>A
c.926T>A (p.Leu309His)
8g.144414038G>ACA372619958SLC39A4c.1207C>T (p.Leu403Phe)
c.1132C>T (p.Leu378Phe)
n.44C>T
c.925C>T (p.Leu309Phe)
 gnomAD v4
8g.144414038G>CCA372619960SLC39A4c.1207C>G (p.Leu403Val)
c.1132C>G (p.Leu378Val)
n.44C>G
c.925C>G (p.Leu309Val)
8g.144414038G>TCA372619962SLC39A4c.1207C>A (p.Leu403Ile)
c.1132C>A (p.Leu378Ile)
n.44C>A
c.925C>A (p.Leu309Ile)
8g.144414039G>ACA463556142SLC39A4c.1206C>T (p.Arg402=)
c.1131C>T (p.Arg377=)
n.43C>T
c.924C>T (p.Arg308=)
8g.144414039G>CCA463556143SLC39A4c.1206C>G (p.Arg402=)
c.1131C>G (p.Arg377=)
n.43C>G
c.924C>G (p.Arg308=)
8g.144414039G>TCA463556146SLC39A4c.1206C>A (p.Arg402=)
c.1131C>A (p.Arg377=)
n.43C>A
c.924C>A (p.Arg308=)
8g.144414040C>ACA372619968SLC39A4c.1205G>T (p.Arg402Leu)
c.1130G>T (p.Arg377Leu)
n.42G>T
c.923G>T (p.Arg308Leu)
 gnomAD v4
8g.144414040C=CA1826306903SLC39A4c.1205G= (p.Arg402=)
c.1130G= (p.Arg377=)
n.42G=
c.923G= (p.Arg308=)
8g.144414040C>GCA372619966SLC39A4c.1205G>C (p.Arg402Pro)
c.1130G>C (p.Arg377Pro)
n.42G>C
c.923G>C (p.Arg308Pro)
8g.144414040C>TCA4941327SLC39A4c.1205G>A (p.Arg402His)
c.1130G>A (p.Arg377His)
n.42G>A
c.923G>A (p.Arg308His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414041G>ACA4941328SLC39A4c.1204C>T (p.Arg402Cys)
c.1129C>T (p.Arg377Cys)
n.41C>T
c.922C>T (p.Arg308Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414041G>CCA372619972SLC39A4c.1204C>G (p.Arg402Gly)
c.1129C>G (p.Arg377Gly)
n.41C>G
c.922C>G (p.Arg308Gly)
8g.144414041G=CA1826306904SLC39A4c.1204C= (p.Arg402=)
c.1129C= (p.Arg377=)
n.41C=
c.922C= (p.Arg308=)
8g.144414041G>TCA372619975SLC39A4c.1204C>A (p.Arg402Ser)
c.1129C>A (p.Arg377Ser)
n.41C>A
c.922C>A (p.Arg308Ser)
 dbSNP gnomAD v3 gnomAD v4
8g.144414042C>ACA372619978SLC39A4c.1203G>T (p.Trp401Cys)
c.1128G>T (p.Trp376Cys)
n.40G>T
c.921G>T (p.Trp307Cys)
 gnomAD v4
8g.144414042C=CA1826306905SLC39A4c.1203G= (p.Trp401=)
c.1128G= (p.Trp376=)
n.40G=
c.921G= (p.Trp307=)
8g.144414042C>GCA372619981SLC39A4c.1203G>C (p.Trp401Cys)
c.1128G>C (p.Trp376Cys)
n.40G>C
c.921G>C (p.Trp307Cys)
8g.144414042C>TCA187646778SLC39A4c.1203G>A (p.Trp401Ter)
c.1128G>A (p.Trp376Ter)
n.40G>A
c.921G>A (p.Trp307Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414043C>ACA372619986SLC39A4c.1202G>T (p.Trp401Leu)
c.1127G>T (p.Trp376Leu)
n.39G>T
c.920G>T (p.Trp307Leu)
8g.144414043C>GCA372619989SLC39A4c.1202G>C (p.Trp401Ser)
c.1127G>C (p.Trp376Ser)
n.39G>C
c.920G>C (p.Trp307Ser)
8g.144414043C>TCA372619991SLC39A4c.1202G>A (p.Trp401Ter)
c.1127G>A (p.Trp376Ter)
n.39G>A
c.920G>A (p.Trp307Ter)
 ClinVar dbSNP
8g.144414044A>CCA372619993SLC39A4c.1201T>G (p.Trp401Gly)
c.1126T>G (p.Trp376Gly)
n.38T>G
c.919T>G (p.Trp307Gly)
8g.144414044A>GCA372619996SLC39A4c.1201T>C (p.Trp401Arg)
c.1126T>C (p.Trp376Arg)
n.38T>C
c.919T>C (p.Trp307Arg)
 gnomAD v4
8g.144414044A>TCA372619998SLC39A4c.1201T>A (p.Trp401Arg)
c.1126T>A (p.Trp376Arg)
n.38T>A
c.919T>A (p.Trp307Arg)
 gnomAD v4
8g.144414045G>ACA187646779SLC39A4c.1200C>T (p.Thr400=)
c.1125C>T (p.Thr375=)
n.37C>T
c.918C>T (p.Thr306=)
 dbSNP gnomAD v2 gnomAD v4
8g.144414045G>CCA463556151SLC39A4c.1200C>G (p.Thr400=)
c.1125C>G (p.Thr375=)
n.37C>G
c.918C>G (p.Thr306=)
8g.144414045G=CA1826306906SLC39A4c.1200C= (p.Thr400=)
c.1125C= (p.Thr375=)
n.37C=
c.918C= (p.Thr306=)
8g.144414045G>TCA463556152SLC39A4c.1200C>A (p.Thr400=)
c.1125C>A (p.Thr375=)
n.37C>A
c.918C>A (p.Thr306=)
8g.144414046G>ACA372620003SLC39A4c.1199C>T (p.Thr400Ile)
c.1124C>T (p.Thr375Ile)
n.36C>T
c.917C>T (p.Thr306Ile)
 dbSNP gnomAD v4
8g.144414046G>CCA372620005SLC39A4c.1199C>G (p.Thr400Ser)
c.1124C>G (p.Thr375Ser)
n.36C>G
c.917C>G (p.Thr306Ser)
8g.144414046G=CA1826306907SLC39A4c.1199C= (p.Thr400=)
c.1124C= (p.Thr375=)
n.36C=
c.917C= (p.Thr306=)
8g.144414046G>TCA372620007SLC39A4c.1199C>A (p.Thr400Asn)
c.1124C>A (p.Thr375Asn)
n.36C>A
c.917C>A (p.Thr306Asn)
8g.144414054_144414060dupCA463556153SLC39A4c.1193_1199dup (p.Trp401AlafsTer19)
c.1118_1124dup (p.Trp376AlafsTer19)
n.30_36dup
c.911_917dup (p.Trp307AlafsTer19)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414047T>ACA372620011SLC39A4c.1198A>T (p.Thr400Ser)
c.1123A>T (p.Thr375Ser)
n.35A>T
c.916A>T (p.Thr306Ser)
8g.144414047T>CCA372620014SLC39A4c.1198A>G (p.Thr400Ala)
c.1123A>G (p.Thr375Ala)
n.35A>G
c.916A>G (p.Thr306Ala)
 gnomAD v4
8g.144414047T>GCA372620013SLC39A4c.1198A>C (p.Thr400Pro)
c.1123A>C (p.Thr375Pro)
n.35A>C
c.916A>C (p.Thr306Pro)
8g.144414048G>ACA463556160SLC39A4c.1197C>T (p.Pro399=)
c.1122C>T (p.Pro374=)
n.34C>T
c.915C>T (p.Pro305=)
 gnomAD v4
8g.144414048G>CCA463556157SLC39A4c.1197C>G (p.Pro399=)
c.1122C>G (p.Pro374=)
n.34C>G
c.915C>G (p.Pro305=)
8g.144414048G>TCA463556155SLC39A4c.1197C>A (p.Pro399=)
c.1122C>A (p.Pro374=)
n.34C>A
c.915C>A (p.Pro305=)
 gnomAD v4
8g.144414049G>ACA372620018SLC39A4c.1196C>T (p.Pro399Leu)
c.1121C>T (p.Pro374Leu)
n.33C>T
c.914C>T (p.Pro305Leu)
 gnomAD v4
8g.144414049G>CCA372620021SLC39A4c.1196C>G (p.Pro399Arg)
c.1121C>G (p.Pro374Arg)
n.33C>G
c.914C>G (p.Pro305Arg)
8g.144414049G>TCA372620023SLC39A4c.1196C>A (p.Pro399His)
c.1121C>A (p.Pro374His)
n.33C>A
c.914C>A (p.Pro305His)
8g.144414049_144414071delinsGGCTGTGGGCTGAGGCCCTCTTCCA1826306908SLC39A4c.1174_1196delinsGAAGAGGGCCTCAGCCCACAGCC (p.Glu392=)
c.1099_1121delinsGAAGAGGGCCTCAGCCCACAGCC (p.Glu367=)
n.11_33delinsGAAGAGGGCCTCAGCCCACAGCC
c.892_914delinsGAAGAGGGCCTCAGCCCACAGCC (p.Glu298=)
8g.144414050G>ACA372620027SLC39A4c.1195C>T (p.Pro399Ser)
c.1120C>T (p.Pro374Ser)
n.32C>T
c.913C>T (p.Pro305Ser)
8g.144414050G>CCA372620028SLC39A4c.1195C>G (p.Pro399Ala)
c.1120C>G (p.Pro374Ala)
n.32C>G
c.913C>G (p.Pro305Ala)
8g.144414050G>TCA372620030SLC39A4c.1195C>A (p.Pro399Thr)
c.1120C>A (p.Pro374Thr)
n.32C>A
c.913C>A (p.Pro305Thr)
 gnomAD v4
8g.144414056_144414077delCA586163391SLC39A4c.1174_1195del (p.Glu392ProfsTer?)
c.1099_1120del (p.Glu367ProfsTer?)
n.11_32del
c.892_913del (p.Glu298ProfsTer?)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414051C>ACA372620034SLC39A4c.1194G>T (p.Gln398His)
c.1119G>T (p.Gln373His)
n.31G>T
c.912G>T (p.Gln304His)
 gnomAD v4
8g.144414051C>GCA372620036SLC39A4c.1194G>C (p.Gln398His)
c.1119G>C (p.Gln373His)
n.31G>C
c.912G>C (p.Gln304His)
8g.144414051C>TCA463556164SLC39A4c.1194G>A (p.Gln398=)
c.1119G>A (p.Gln373=)
n.31G>A
c.912G>A (p.Gln304=)
8g.144414052T>ACA372620038SLC39A4c.1193A>T (p.Gln398Leu)
c.1118A>T (p.Gln373Leu)
n.30A>T
c.911A>T (p.Gln304Leu)
8g.144414052T>CCA372620040SLC39A4c.1193A>G (p.Gln398Arg)
c.1118A>G (p.Gln373Arg)
n.30A>G
c.911A>G (p.Gln304Arg)
 dbSNP gnomAD v2 gnomAD v4
8g.144414052T>GCA372620042SLC39A4c.1193A>C (p.Gln398Pro)
c.1118A>C (p.Gln373Pro)
n.30A>C
c.911A>C (p.Gln304Pro)
8g.144414052T=CA1826306909SLC39A4c.1193A= (p.Gln398=)
c.1118A= (p.Gln373=)
n.30A=
c.911A= (p.Gln304=)
8g.144414053G>ACA372620046SLC39A4c.1192C>T (p.Gln398Ter)
c.1117C>T (p.Gln373Ter)
n.29C>T
c.910C>T (p.Gln304Ter)
8g.144414053G>CCA372620045SLC39A4c.1192C>G (p.Gln398Glu)
c.1117C>G (p.Gln373Glu)
n.29C>G
c.910C>G (p.Gln304Glu)
 gnomAD v4
8g.144414053G>TCA372620044SLC39A4c.1192C>A (p.Gln398Lys)
c.1117C>A (p.Gln373Lys)
n.29C>A
c.910C>A (p.Gln304Lys)
 gnomAD v4
8g.144414054T>ACA463556165SLC39A4c.1191A>T (p.Pro397=)
c.1116A>T (p.Pro372=)
n.28A>T
c.909A>T (p.Pro303=)
8g.144414054T>CCA4941329SLC39A4c.1191A>G (p.Pro397=)
c.1116A>G (p.Pro372=)
n.28A>G
c.909A>G (p.Pro303=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414054T>GCA463556166SLC39A4c.1191A>C (p.Pro397=)
c.1116A>C (p.Pro372=)
n.28A>C
c.909A>C (p.Pro303=)
8g.144414054T=CA1826306910SLC39A4c.1191A= (p.Pro397=)
c.1116A= (p.Pro372=)
n.28A=
c.909A= (p.Pro303=)
8g.144414055G>ACA372620052SLC39A4c.1190C>T (p.Pro397Leu)
c.1115C>T (p.Pro372Leu)
n.27C>T
c.908C>T (p.Pro303Leu)
8g.144414055G>CCA372620054SLC39A4c.1190C>G (p.Pro397Arg)
c.1115C>G (p.Pro372Arg)
n.27C>G
c.908C>G (p.Pro303Arg)
8g.144414055G>TCA372620057SLC39A4c.1190C>A (p.Pro397Gln)
c.1115C>A (p.Pro372Gln)
n.27C>A
c.908C>A (p.Pro303Gln)
 gnomAD v4
8g.144414057dupCA2695210375SLC39A4c.1190dup (p.Gln398ThrfsTer20)
c.1115dup (p.Gln373ThrfsTer20)
n.27dup
c.908dup (p.Gln304ThrfsTer20)
8g.144414056G>ACA372620060SLC39A4c.1189C>T (p.Pro397Ser)
c.1114C>T (p.Pro372Ser)
n.26C>T
c.907C>T (p.Pro303Ser)
8g.144414056G>CCA372620063SLC39A4c.1189C>G (p.Pro397Ala)
c.1114C>G (p.Pro372Ala)
n.26C>G
c.907C>G (p.Pro303Ala)
8g.144414056G>TCA372620065SLC39A4c.1189C>A (p.Pro397Thr)
c.1114C>A (p.Pro372Thr)
n.26C>A
c.907C>A (p.Pro303Thr)
8g.144414057G>ACA463556171SLC39A4c.1188C>T (p.Ser396=)
c.1113C>T (p.Ser371=)
n.25C>T
c.906C>T (p.Ser302=)
 gnomAD v4
8g.144414057G>CCA187646781SLC39A4c.1188C>G (p.Ser396Arg)
c.1113C>G (p.Ser371Arg)
n.25C>G
c.906C>G (p.Ser302Arg)
 dbSNP
8g.144414057G=CA1826306911SLC39A4c.1188C= (p.Ser396=)
c.1113C= (p.Ser371=)
n.25C=
c.906C= (p.Ser302=)
8g.144414057G>TCA372620068SLC39A4c.1188C>A (p.Ser396Arg)
c.1113C>A (p.Ser371Arg)
n.25C>A
c.906C>A (p.Ser302Arg)
8g.144414058C>ACA372620072SLC39A4c.1187G>T (p.Ser396Ile)
c.1112G>T (p.Ser371Ile)
n.24G>T
c.905G>T (p.Ser302Ile)
8g.144414058C>GCA372620074SLC39A4c.1187G>C (p.Ser396Thr)
c.1112G>C (p.Ser371Thr)
n.24G>C
c.905G>C (p.Ser302Thr)
8g.144414058C>TCA372620075SLC39A4c.1187G>A (p.Ser396Asn)
c.1112G>A (p.Ser371Asn)
n.24G>A
c.905G>A (p.Ser302Asn)
8g.144414059T>ACA372620078SLC39A4c.1186A>T (p.Ser396Cys)
c.1111A>T (p.Ser371Cys)
n.23A>T
c.904A>T (p.Ser302Cys)
8g.144414059T>CCA372620081SLC39A4c.1186A>G (p.Ser396Gly)
c.1111A>G (p.Ser371Gly)
n.23A>G
c.904A>G (p.Ser302Gly)
8g.144414059T>GCA372620083SLC39A4c.1186A>C (p.Ser396Arg)
c.1111A>C (p.Ser371Arg)
n.23A>C
c.904A>C (p.Ser302Arg)
8g.144414060G>ACA463556172SLC39A4c.1185C>T (p.Leu395=)
c.1110C>T (p.Leu370=)
n.22C>T
c.903C>T (p.Leu301=)
 gnomAD v4
8g.144414060G>CCA463556173SLC39A4c.1185C>G (p.Leu395=)
c.1110C>G (p.Leu370=)
n.22C>G
c.903C>G (p.Leu301=)
8g.144414060G>TCA463556174SLC39A4c.1185C>A (p.Leu395=)
c.1110C>A (p.Leu370=)
n.22C>A
c.903C>A (p.Leu301=)
8g.144414061A=CA1826306912SLC39A4c.1184T= (p.Leu395=)
c.1109T= (p.Leu370=)
n.21T=
c.902T= (p.Leu301=)
8g.144414061A>CCA372620084SLC39A4c.1184T>G (p.Leu395Arg)
c.1109T>G (p.Leu370Arg)
n.21T>G
c.902T>G (p.Leu301Arg)
 dbSNP gnomAD v4
8g.144414061A>GCA372620088SLC39A4c.1184T>C (p.Leu395Pro)
c.1109T>C (p.Leu370Pro)
n.21T>C
c.902T>C (p.Leu301Pro)
8g.144414061A>TCA372620086SLC39A4c.1184T>A (p.Leu395His)
c.1109T>A (p.Leu370His)
n.21T>A
c.902T>A (p.Leu301His)
 gnomAD v4
8g.144414062G>ACA372620091SLC39A4c.1183C>T (p.Leu395Phe)
c.1108C>T (p.Leu370Phe)
n.20C>T
c.901C>T (p.Leu301Phe)
8g.144414062G>CCA372620093SLC39A4c.1183C>G (p.Leu395Val)
c.1108C>G (p.Leu370Val)
n.20C>G
c.901C>G (p.Leu301Val)
8g.144414062G>TCA372620095SLC39A4c.1183C>A (p.Leu395Ile)
c.1108C>A (p.Leu370Ile)
n.20C>A
c.901C>A (p.Leu301Ile)
8g.144414063G>ACA463556177SLC39A4c.1182C>T (p.Gly394=)
c.1107C>T (p.Gly369=)
n.19C>T
c.900C>T (p.Gly300=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
8g.144414063G>CCA463556176SLC39A4c.1182C>G (p.Gly394=)
c.1107C>G (p.Gly369=)
n.19C>G
c.900C>G (p.Gly300=)
 gnomAD v3 gnomAD v4
8g.144414063G=CA1826306913SLC39A4c.1182C= (p.Gly394=)
c.1107C= (p.Gly369=)
n.19C=
c.900C= (p.Gly300=)
8g.144414063G>TCA463556175SLC39A4c.1182C>A (p.Gly394=)
c.1107C>A (p.Gly369=)
n.19C>A
c.900C>A (p.Gly300=)
8g.144414064C>ACA372620099SLC39A4c.1181G>T (p.Gly394Val)
c.1106G>T (p.Gly369Val)
n.18G>T
c.899G>T (p.Gly300Val)
 dbSNP gnomAD v2
8g.144414064C=CA1826306914SLC39A4c.1181G= (p.Gly394=)
c.1106G= (p.Gly369=)
n.18G=
c.899G= (p.Gly300=)
8g.144414064C>GCA372620101SLC39A4c.1181G>C (p.Gly394Ala)
c.1106G>C (p.Gly369Ala)
n.18G>C
c.899G>C (p.Gly300Ala)
8g.144414064C>TCA372620102SLC39A4c.1181G>A (p.Gly394Asp)
c.1106G>A (p.Gly369Asp)
n.18G>A
c.899G>A (p.Gly300Asp)
 dbSNP gnomAD v2 gnomAD v4
8g.144414065C>ACA372620106SLC39A4c.1180G>T (p.Gly394Cys)
c.1105G>T (p.Gly369Cys)
n.17G>T
c.898G>T (p.Gly300Cys)
8g.144414065C=CA1826306915SLC39A4c.1180G= (p.Gly394=)
c.1105G= (p.Gly369=)
n.17G=
c.898G= (p.Gly300=)
8g.144414065C>GCA372620108SLC39A4c.1180G>C (p.Gly394Arg)
c.1105G>C (p.Gly369Arg)
n.17G>C
c.898G>C (p.Gly300Arg)
8g.144414065C>TCA187646788SLC39A4c.1180G>A (p.Gly394Ser)
c.1105G>A (p.Gly369Ser)
n.17G>A
c.898G>A (p.Gly300Ser)
 dbSNP gnomAD v4
8g.144414066C>ACA372620113SLC39A4c.1179G>T (p.Glu393Asp)
c.1104G>T (p.Glu368Asp)
n.16G>T
c.897G>T (p.Glu299Asp)
8g.144414066C=CA1826306916SLC39A4c.1179G= (p.Glu393=)
c.1104G= (p.Glu368=)
n.16G=
c.897G= (p.Glu299=)
8g.144414066C>GCA372620115SLC39A4c.1179G>C (p.Glu393Asp)
c.1104G>C (p.Glu368Asp)
n.16G>C
c.897G>C (p.Glu299Asp)
 dbSNP gnomAD v4
8g.144414066C>TCA4941330SLC39A4c.1179G>A (p.Glu393=)
c.1104G>A (p.Glu368=)
n.16G>A
c.897G>A (p.Glu299=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414067T>ACA372620122SLC39A4c.1178A>T (p.Glu393Val)
c.1103A>T (p.Glu368Val)
n.15A>T
c.896A>T (p.Glu299Val)
8g.144414067T>CCA372620124SLC39A4c.1178A>G (p.Glu393Gly)
c.1103A>G (p.Glu368Gly)
n.15A>G
c.896A>G (p.Glu299Gly)
 gnomAD v4
8g.144414067T>GCA372620120SLC39A4c.1178A>C (p.Glu393Ala)
c.1103A>C (p.Glu368Ala)
n.15A>C
c.896A>C (p.Glu299Ala)
8g.144414068C>ACA372620128SLC39A4c.1177G>T (p.Glu393Ter)
c.1102G>T (p.Glu368Ter)
n.14G>T
c.895G>T (p.Glu299Ter)
 gnomAD v4
8g.144414068C>GCA372620132SLC39A4c.1177G>C (p.Glu393Gln)
c.1102G>C (p.Glu368Gln)
n.14G>C
c.895G>C (p.Glu299Gln)
8g.144414068C>TCA372620130SLC39A4c.1177G>A (p.Glu393Lys)
c.1102G>A (p.Glu368Lys)
n.14G>A
c.895G>A (p.Glu299Lys)
 gnomAD v4
8g.144414069T>ACA372620135SLC39A4c.1176A>T (p.Glu392Asp)
c.1101A>T (p.Glu367Asp)
n.13A>T
c.894A>T (p.Glu298Asp)
8g.144414069T>CCA463556182SLC39A4c.1176A>G (p.Glu392=)
c.1101A>G (p.Glu367=)
n.13A>G
c.894A>G (p.Glu298=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414069T>GCA372620137SLC39A4c.1176A>C (p.Glu392Asp)
c.1101A>C (p.Glu367Asp)
n.13A>C
c.894A>C (p.Glu298Asp)
 gnomAD v4
8g.144414069T=CA1826306917SLC39A4c.1176A= (p.Glu392=)
c.1101A= (p.Glu367=)
n.13A=
c.894A= (p.Glu298=)
8g.144414070T>ACA372620141SLC39A4c.1175A>T (p.Glu392Val)
c.1100A>T (p.Glu367Val)
n.12A>T
c.893A>T (p.Glu298Val)
8g.144414070T>CCA372620142SLC39A4c.1175A>G (p.Glu392Gly)
c.1100A>G (p.Glu367Gly)
n.12A>G
c.893A>G (p.Glu298Gly)
8g.144414070T>GCA372620144SLC39A4c.1175A>C (p.Glu392Ala)
c.1100A>C (p.Glu367Ala)
n.12A>C
c.893A>C (p.Glu298Ala)
8g.144414071C>ACA372620148SLC39A4c.1174G>T (p.Glu392Ter)
c.1099G>T (p.Glu367Ter)
n.11G>T
c.892G>T (p.Glu298Ter)
 gnomAD v4
8g.144414071C=CA1826306918SLC39A4c.1174G= (p.Glu392=)
c.1099G= (p.Glu367=)
n.11G=
c.892G= (p.Glu298=)
8g.144414071C>GCA4941332SLC39A4c.1174G>C (p.Glu392Gln)
c.1099G>C (p.Glu367Gln)
n.11G>C
c.892G>C (p.Glu298Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414071C>TCA4941331SLC39A4c.1174G>A (p.Glu392Lys)
c.1099G>A (p.Glu367Lys)
n.11G>A
c.892G>A (p.Glu298Lys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414072G>ACA4941333SLC39A4c.1173C>T (p.Ser391=)
c.1098C>T (p.Ser366=)
n.10C>T
c.891C>T (p.Ser297=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414072G>CCA187646842SLC39A4c.1173C>G (p.Ser391Arg)
c.1098C>G (p.Ser366Arg)
n.10C>G
c.891C>G (p.Ser297Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414072G=CA1826306919SLC39A4c.1173C= (p.Ser391=)
c.1098C= (p.Ser366=)
n.10C=
c.891C= (p.Ser297=)
8g.144414072G>TCA372620157SLC39A4c.1173C>A (p.Ser391Arg)
c.1098C>A (p.Ser366Arg)
n.10C>A
c.891C>A (p.Ser297Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414073C>ACA372620165SLC39A4c.1172G>T (p.Ser391Ile)
c.1097G>T (p.Ser366Ile)
n.9G>T
c.890G>T (p.Ser297Ile)
 gnomAD v4
8g.144414073C=CA1826306920SLC39A4c.1172G= (p.Ser391=)
c.1097G= (p.Ser366=)
n.9G=
c.890G= (p.Ser297=)
8g.144414073C>GCA372620161SLC39A4c.1172G>C (p.Ser391Thr)
c.1097G>C (p.Ser366Thr)
n.9G>C
c.890G>C (p.Ser297Thr)
8g.144414073C>TCA372620163SLC39A4c.1172G>A (p.Ser391Asn)
c.1097G>A (p.Ser366Asn)
n.9G>A
c.890G>A (p.Ser297Asn)
 dbSNP gnomAD v4
8g.144414074T>ACA372620167SLC39A4c.1171A>T (p.Ser391Cys)
c.1096A>T (p.Ser366Cys)
n.8A>T
c.889A>T (p.Ser297Cys)
8g.144414074T>CCA372620169SLC39A4c.1171A>G (p.Ser391Gly)
c.1096A>G (p.Ser366Gly)
n.8A>G
c.889A>G (p.Ser297Gly)
 dbSNP gnomAD v4
8g.144414074T>GCA372620171SLC39A4c.1171A>C (p.Ser391Arg)
c.1096A>C (p.Ser366Arg)
n.8A>C
c.889A>C (p.Ser297Arg)
8g.144414074T=CA1826306921SLC39A4c.1171A= (p.Ser391=)
c.1096A= (p.Ser366=)
n.8A=
c.889A= (p.Ser297=)
8g.144414079_144414080delCA2689097752SLC39A4c.1170_1171del (p.His390GlnfsTer27)
c.1095_1096del (p.His365GlnfsTer27)
n.7_8del
c.888_889del (p.His296GlnfsTer27)
 gnomAD v4
8g.144414075G>ACA463556190SLC39A4c.1170C>T (p.His390=)
c.1095C>T (p.His365=)
n.7C>T
c.888C>T (p.His296=)
 ClinVar dbSNP gnomAD v4
8g.144414075G>CCA372620174SLC39A4c.1170C>G (p.His390Gln)
c.1095C>G (p.His365Gln)
n.7C>G
c.888C>G (p.His296Gln)
 gnomAD v4
8g.144414075G=CA1826306922SLC39A4c.1170C= (p.His390=)
c.1095C= (p.His365=)
n.7C=
c.888C= (p.His296=)
8g.144414075G>TCA372620176SLC39A4c.1170C>A (p.His390Gln)
c.1095C>A (p.His365Gln)
n.7C>A
c.888C>A (p.His296Gln)
8g.144414076T>ACA372620179SLC39A4c.1169A>T (p.His390Leu)
c.1094A>T (p.His365Leu)
n.6A>T
c.887A>T (p.His296Leu)
8g.144414076T>CCA372620180SLC39A4c.1169A>G (p.His390Arg)
c.1094A>G (p.His365Arg)
n.6A>G
c.887A>G (p.His296Arg)
8g.144414076T>GCA372620181SLC39A4c.1169A>C (p.His390Pro)
c.1094A>C (p.His365Pro)
n.6A>C
c.887A>C (p.His296Pro)
8g.144414077G>ACA372620184SLC39A4c.1168C>T (p.His390Tyr)
c.1093C>T (p.His365Tyr)
n.5C>T
c.886C>T (p.His296Tyr)
8g.144414077G>CCA372620186SLC39A4c.1168C>G (p.His390Asp)
c.1093C>G (p.His365Asp)
n.5C>G
c.886C>G (p.His296Asp)
8g.144414077G>TCA372620188SLC39A4c.1168C>A (p.His390Asn)
c.1093C>A (p.His365Asn)
n.5C>A
c.886C>A (p.His296Asn)
8g.144414078T>ACA463556194SLC39A4c.1167A>T (p.Thr389=)
c.1092A>T (p.Thr364=)
n.4A>T
c.885A>T (p.Thr295=)
8g.144414078T>CCA463556195SLC39A4c.1167A>G (p.Thr389=)
c.1092A>G (p.Thr364=)
n.4A>G
c.885A>G (p.Thr295=)
8g.144414078T>GCA463556196SLC39A4c.1167A>C (p.Thr389=)
c.1092A>C (p.Thr364=)
n.4A>C
c.885A>C (p.Thr295=)
8g.144414079G>ACA372620193SLC39A4c.1166C>T (p.Thr389Ile)
c.1091C>T (p.Thr364Ile)
n.3C>T
c.884C>T (p.Thr295Ile)
 gnomAD v4
8g.144414079G>CCA372620195SLC39A4c.1166C>G (p.Thr389Arg)
c.1091C>G (p.Thr364Arg)
n.3C>G
c.884C>G (p.Thr295Arg)
8g.144414079G>TCA372620191SLC39A4c.1166C>A (p.Thr389Lys)
c.1091C>A (p.Thr364Lys)
n.3C>A
c.884C>A (p.Thr295Lys)
8g.144414080T>ACA372620198SLC39A4c.1165A>T (p.Thr389Ser)
c.1090A>T (p.Thr364Ser)
n.2A>T
c.883A>T (p.Thr295Ser)
8g.144414080T>CCA372620201SLC39A4c.1165A>G (p.Thr389Ala)
c.1090A>G (p.Thr364Ala)
n.2A>G
c.883A>G (p.Thr295Ala)
8g.144414080T>GCA372620203SLC39A4c.1165A>C (p.Thr389Pro)
c.1090A>C (p.Thr364Pro)
n.2A>C
c.883A>C (p.Thr295Pro)
8g.144414081A>CCA372620206SLC39A4c.1164T>G (p.His388Gln)
c.1089T>G (p.His363Gln)
n.1T>G
c.882T>G (p.His294Gln)
8g.144414081A>GCA463556198SLC39A4c.1164T>C (p.His388=)
c.1089T>C (p.His363=)
n.1T>C
c.882T>C (p.His294=)
 ClinVar
8g.144414081A>TCA372620208SLC39A4c.1164T>A (p.His388Gln)
c.1089T>A (p.His363Gln)
n.1T>A
c.882T>A (p.His294Gln)
8g.144414082_144414085delCA2689097763SLC39A4c.1161_1164del (p.His390AlafsTer?)
c.1086_1089del (p.His365AlafsTer?)
c.879_882del (p.His296AlafsTer?)
 gnomAD v4
8g.144414082T>ACA372620212SLC39A4c.1163A>T (p.His388Leu)
c.1088A>T (p.His363Leu)
c.881A>T (p.His294Leu)
8g.144414082T>CCA372620214SLC39A4c.1163A>G (p.His388Arg)
c.1088A>G (p.His363Arg)
c.881A>G (p.His294Arg)
 gnomAD v4
8g.144414082T>GCA372620217SLC39A4c.1163A>C (p.His388Pro)
c.1088A>C (p.His363Pro)
c.881A>C (p.His294Pro)
8g.144414083G>ACA372620220SLC39A4c.1162C>T (p.His388Tyr)
c.1087C>T (p.His363Tyr)
c.880C>T (p.His294Tyr)
 gnomAD v4
8g.144414083G>CCA372620222SLC39A4c.1162C>G (p.His388Asp)
c.1087C>G (p.His363Asp)
c.880C>G (p.His294Asp)
 dbSNP gnomAD v2
8g.144414083G=CA1826306923SLC39A4c.1162C= (p.His388=)
c.1087C= (p.His363=)
c.880C= (p.His294=)
8g.144414083G>TCA372620224SLC39A4c.1162C>A (p.His388Asn)
c.1087C>A (p.His363Asn)
c.880C>A (p.His294Asn)
8g.144414084C>ACA463556201SLC39A4c.1161G>T (p.Leu387=)
c.1086G>T (p.Leu362=)
c.879G>T (p.Leu293=)
8g.144414084C>GCA463556203SLC39A4c.1161G>C (p.Leu387=)
c.1086G>C (p.Leu362=)
c.879G>C (p.Leu293=)
8g.144414084C>TCA463556205SLC39A4c.1161G>A (p.Leu387=)
c.1086G>A (p.Leu362=)
c.879G>A (p.Leu293=)
8g.144414085A=CA1826306924SLC39A4c.1160T= (p.Leu387=)
c.1085T= (p.Leu362=)
c.878T= (p.Leu293=)
8g.144414085A>CCA372620229SLC39A4c.1160T>G (p.Leu387Arg)
c.1085T>G (p.Leu362Arg)
c.878T>G (p.Leu293Arg)
8g.144414085A>GCA372620231SLC39A4c.1160T>C (p.Leu387Pro)
c.1085T>C (p.Leu362Pro)
c.878T>C (p.Leu293Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v4
8g.144414085A>TCA372620232SLC39A4c.1160T>A (p.Leu387Gln)
c.1085T>A (p.Leu362Gln)
c.878T>A (p.Leu293Gln)
 dbSNP gnomAD v3 gnomAD v4
8g.144414086G>ACA463556206SLC39A4c.1159C>T (p.Leu387=)
c.1084C>T (p.Leu362=)
c.877C>T (p.Leu293=)
 dbSNP gnomAD v3 gnomAD v4
8g.144414086G>CCA372620234SLC39A4c.1159C>G (p.Leu387Val)
c.1084C>G (p.Leu362Val)
c.877C>G (p.Leu293Val)
8g.144414086G=CA1826306925SLC39A4c.1159C= (p.Leu387=)
c.1084C= (p.Leu362=)
c.877C= (p.Leu293=)
8g.144414086G>TCA372620236SLC39A4c.1159C>A (p.Leu387Met)
c.1084C>A (p.Leu362Met)
c.877C>A (p.Leu293Met)
8g.144414087C>ACA463556207SLC39A4c.1158G>T (p.Gly386=)
c.1083G>T (p.Gly361=)
c.876G>T (p.Gly292=)
 gnomAD v4
8g.144414087C=CA1826306926SLC39A4c.1158G= (p.Gly386=)
c.1083G= (p.Gly361=)
c.876G= (p.Gly292=)
8g.144414087C>GCA463556208SLC39A4c.1158G>C (p.Gly386=)
c.1083G>C (p.Gly361=)
c.876G>C (p.Gly292=)
8g.144414087C>TCA463556209SLC39A4c.1158G>A (p.Gly386=)
c.1083G>A (p.Gly361=)
c.876G>A (p.Gly292=)
 ClinVar dbSNP gnomAD v4
8g.144414088C>ACA372620239SLC39A4c.1157G>T (p.Gly386Val)
c.1082G>T (p.Gly361Val)
c.875G>T (p.Gly292Val)
8g.144414088C>GCA372620242SLC39A4c.1157G>C (p.Gly386Ala)
c.1082G>C (p.Gly361Ala)
c.875G>C (p.Gly292Ala)
8g.144414088C>TCA372620244SLC39A4c.1157G>A (p.Gly386Glu)
c.1082G>A (p.Gly361Glu)
c.875G>A (p.Gly292Glu)
8g.144414089C>ACA372620247SLC39A4c.1156G>T (p.Gly386Trp)
c.1081G>T (p.Gly361Trp)
c.874G>T (p.Gly292Trp)
8g.144414089C=CA1826306927SLC39A4c.1156G= (p.Gly386=)
c.1081G= (p.Gly361=)
c.874G= (p.Gly292=)
8g.144414089C>GCA372620249SLC39A4c.1156G>C (p.Gly386Arg)
c.1081G>C (p.Gly361Arg)
c.874G>C (p.Gly292Arg)
8g.144414089C>TCA4941334SLC39A4c.1156G>A (p.Gly386Arg)
c.1081G>A (p.Gly361Arg)
c.874G>A (p.Gly292Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414090C>ACA4941335SLC39A4c.1155G>T (p.Leu385=)
c.1080G>T (p.Leu360=)
c.873G>T (p.Leu291=)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414090C=CA1826306928SLC39A4c.1155G= (p.Leu385=)
c.1080G= (p.Leu360=)
c.873G= (p.Leu291=)
8g.144414090C>GCA463556214SLC39A4c.1155G>C (p.Leu385=)
c.1080G>C (p.Leu360=)
c.873G>C (p.Leu291=)
8g.144414090C>TCA463556215SLC39A4c.1155G>A (p.Leu385=)
c.1080G>A (p.Leu360=)
c.873G>A (p.Leu291=)
 dbSNP
8g.144414091A=CA1826306929SLC39A4c.1154T= (p.Leu385=)
c.1079T= (p.Leu360=)
c.872T= (p.Leu291=)
8g.144414091A>CCA372620255SLC39A4c.1154T>G (p.Leu385Arg)
c.1079T>G (p.Leu360Arg)
c.872T>G (p.Leu291Arg)
8g.144414091A>GCA4941336SLC39A4c.1154T>C (p.Leu385Pro)
c.1079T>C (p.Leu360Pro)
c.872T>C (p.Leu291Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414091A>TCA372620259SLC39A4c.1154T>A (p.Leu385Gln)
c.1079T>A (p.Leu360Gln)
c.872T>A (p.Leu291Gln)

Number of alleles fetched