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.144414251_144414265delinsTGGGGGCAGACCTTGCA1826307047SLC39A4c.1146_1149+11delinsCAAGGTCTGCCCCCA
c.1071_1074+11delinsCAAGGTCTGCCCCCA
c.864_867+11delinsCAAGGTCTGCCCCCA
8g.144414256dupCA848876150SLC39A4c.1149+10dup (n.1149+10dup)
c.1074+10dup (n.1074+10dup)
c.867+10dup (n.867+10dup)
 ClinVar dbSNP gnomAD v3 gnomAD v4
8g.144414256delCA1826307048SLC39A4c.1149+10del (n.1149+10del)
c.1074+10del (n.1074+10del)
c.867+10del (n.867+10del)
 ClinVar dbSNP gnomAD v4
8g.144414254_144414267delCA1139660827SLC39A4c.1146_1149+10del
c.1071_1074+10del
c.864_867+10del
 ClinVar dbSNP
8g.144414253G>ACA4941383SLC39A4c.1149+9C>T (n.1149+9C>T)
c.1074+9C>T (n.1074+9C>T)
c.867+9C>T (n.867+9C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414253G=CA1826307050SLC39A4c.1149+9C= (n.1149+9C=)
c.1074+9C= (n.1074+9C=)
c.867+9C= (n.867+9C=)
8g.144414254G>ACA4941384SLC39A4c.1149+8C>T (n.1149+8C>T)
c.1074+8C>T (n.1074+8C>T)
c.867+8C>T (n.867+8C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414254G>CCA4941385SLC39A4c.1149+8C>G (n.1149+8C>G)
c.1074+8C>G (n.1074+8C>G)
c.867+8C>G (n.867+8C>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414254G=CA1826307051SLC39A4c.1149+8C= (n.1149+8C=)
c.1074+8C= (n.1074+8C=)
c.867+8C= (n.867+8C=)
8g.144414255G>ACA4941386SLC39A4c.1149+7C>T (n.1149+7C>T)
c.1074+7C>T (n.1074+7C>T)
c.867+7C>T (n.867+7C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414255G=CA1826307052SLC39A4c.1149+7C= (n.1149+7C=)
c.1074+7C= (n.1074+7C=)
c.867+7C= (n.867+7C=)
8g.144414255_144414256insACA2579281043SLC39A4c.1149+6_1149+7insT (n.1149+6_1149+7insT)
c.1074+6_1074+7insT (n.1074+6_1074+7insT)
c.867+6_867+7insT (n.867+6_867+7insT)
 ClinVar gnomAD v4
8g.144414256G>ACA586164227SLC39A4c.1149+6C>T (n.1149+6C>T)
c.1074+6C>T (n.1074+6C>T)
c.867+6C>T (n.867+6C>T)
 dbSNP gnomAD v2 gnomAD v4
8g.144414256G=CA1826307053SLC39A4c.1149+6C= (n.1149+6C=)
c.1074+6C= (n.1074+6C=)
c.867+6C= (n.867+6C=)
8g.144414257C>ACA2689098363SLC39A4c.1149+5G>T (n.1149+5G>T)
c.1074+5G>T (n.1074+5G>T)
c.867+5G>T (n.867+5G>T)
 gnomAD v4
8g.144414257C>TCA2689098364SLC39A4c.1149+5G>A (n.1149+5G>A)
c.1074+5G>A (n.1074+5G>A)
c.867+5G>A (n.867+5G>A)
 gnomAD v4
8g.144414258A=CA1826307054SLC39A4c.1149+4T= (n.1149+4T=)
c.1074+4T= (n.1074+4T=)
c.867+4T= (n.867+4T=)
8g.144414258A>GCA586164228SLC39A4c.1149+4T>C (n.1149+4T>C)
c.1074+4T>C (n.1074+4T>C)
c.867+4T>C (n.867+4T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414259G>TCA2689098370SLC39A4c.1149+3C>A (n.1149+3C>A)
c.1074+3C>A (n.1074+3C>A)
c.867+3C>A (n.867+3C>A)
 gnomAD v4
8g.144414259dupCA2689098369SLC39A4c.1149+3dup (n.1149+3dup)
c.1074+3dup (n.1074+3dup)
c.867+3dup (n.867+3dup)
 gnomAD v4
8g.144414260A=CA1826307055SLC39A4c.1149+2T= (n.1149+2T=)
c.1074+2T= (n.1074+2T=)
c.867+2T= (n.867+2T=)
8g.144414260A>CCA372621072SLC39A4c.1149+2T>G (n.1149+2T>G)
c.1074+2T>G (n.1074+2T>G)
c.867+2T>G (n.867+2T>G)
8g.144414260A>GCA372621070SLC39A4c.1149+2T>C (n.1149+2T>C)
c.1074+2T>C (n.1074+2T>C)
c.867+2T>C (n.867+2T>C)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414260A>TCA372621071SLC39A4c.1149+2T>A (n.1149+2T>A)
c.1074+2T>A (n.1074+2T>A)
c.867+2T>A (n.867+2T>A)
8g.144414261C>ACA372621073SLC39A4c.1149+1G>T (n.1149+1G>T)
c.1074+1G>T (n.1074+1G>T)
c.867+1G>T (n.867+1G>T)
 ClinVar gnomAD v4
8g.144414261C>GCA372621074SLC39A4c.1149+1G>C (n.1149+1G>C)
c.1074+1G>C (n.1074+1G>C)
c.867+1G>C (n.867+1G>C)
 gnomAD v4
8g.144414261C>TCA372621075SLC39A4c.1149+1G>A (n.1149+1G>A)
c.1074+1G>A (n.1074+1G>A)
c.867+1G>A (n.867+1G>A)
 ClinVar gnomAD v4
8g.144414262C>ACA372621076SLC39A4c.1149G>T (p.Lys383Asn)
c.1074G>T (p.Lys358Asn)
c.867G>T (p.Lys289Asn)
 gnomAD v4
8g.144414262C>GCA372621077SLC39A4c.1149G>C (p.Lys383Asn)
c.1074G>C (p.Lys358Asn)
c.867G>C (p.Lys289Asn)
 gnomAD v4
8g.144414262C>TCA463449570SLC39A4c.1149G>A (p.Lys383=)
c.1074G>A (p.Lys358=)
c.867G>A (p.Lys289=)
8g.144414263T>ACA372621078SLC39A4c.1148A>T (p.Lys383Met)
c.1073A>T (p.Lys358Met)
c.866A>T (p.Lys289Met)
8g.144414263T>CCA372621079SLC39A4c.1148A>G (p.Lys383Arg)
c.1073A>G (p.Lys358Arg)
c.866A>G (p.Lys289Arg)
8g.144414263T>GCA372621080SLC39A4c.1148A>C (p.Lys383Thr)
c.1073A>C (p.Lys358Thr)
c.866A>C (p.Lys289Thr)
 gnomAD v4
8g.144414264T>ACA372621081SLC39A4c.1147A>T (p.Lys383Ter)
c.1072A>T (p.Lys358Ter)
c.865A>T (p.Lys289Ter)
8g.144414264T>CCA372621082SLC39A4c.1147A>G (p.Lys383Glu)
c.1072A>G (p.Lys358Glu)
c.865A>G (p.Lys289Glu)
 gnomAD v4
8g.144414264T>GCA372621083SLC39A4c.1147A>C (p.Lys383Gln)
c.1072A>C (p.Lys358Gln)
c.865A>C (p.Lys289Gln)
8g.144414265G>ACA463449571SLC39A4c.1146C>T (p.Pro382=)
c.1071C>T (p.Pro357=)
c.864C>T (p.Pro288=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414265G>CCA463449572SLC39A4c.1146C>G (p.Pro382=)
c.1071C>G (p.Pro357=)
c.864C>G (p.Pro288=)
 dbSNP gnomAD v2 gnomAD v4
8g.144414265G=CA1826307056SLC39A4c.1146C= (p.Pro382=)
c.1071C= (p.Pro357=)
c.864C= (p.Pro288=)
8g.144414265G>TCA463449573SLC39A4c.1146C>A (p.Pro382=)
c.1071C>A (p.Pro357=)
c.864C>A (p.Pro288=)
8g.144414267delCA2689098391SLC39A4c.1146del (p.Lys383ArgfsTer?)
c.1071del (p.Lys358ArgfsTer?)
c.864del (p.Lys289ArgfsTer?)
 gnomAD v4
8g.144414266G>ACA372621084SLC39A4c.1145C>T (p.Pro382Leu)
c.1070C>T (p.Pro357Leu)
c.863C>T (p.Pro288Leu)
8g.144414266G>CCA372621086SLC39A4c.1145C>G (p.Pro382Arg)
c.1070C>G (p.Pro357Arg)
c.863C>G (p.Pro288Arg)
8g.144414266G>TCA372621085SLC39A4c.1145C>A (p.Pro382His)
c.1070C>A (p.Pro357His)
c.863C>A (p.Pro288His)
 gnomAD v4
8g.144414267G>ACA372621087SLC39A4c.1144C>T (p.Pro382Ser)
c.1069C>T (p.Pro357Ser)
c.862C>T (p.Pro288Ser)
 dbSNP gnomAD v2 gnomAD v4
8g.144414267G>CCA372621088SLC39A4c.1144C>G (p.Pro382Ala)
c.1069C>G (p.Pro357Ala)
c.862C>G (p.Pro288Ala)
8g.144414267G=CA1826307057SLC39A4c.1144C= (p.Pro382=)
c.1069C= (p.Pro357=)
c.862C= (p.Pro288=)
8g.144414267G>TCA372621089SLC39A4c.1144C>A (p.Pro382Thr)
c.1069C>A (p.Pro357Thr)
c.862C>A (p.Pro288Thr)
 gnomAD v4
8g.144414268C>ACA463449574SLC39A4c.1143G>T (p.Thr381=)
c.1068G>T (p.Thr356=)
c.861G>T (p.Thr287=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414268C=CA1826307058SLC39A4c.1143G= (p.Thr381=)
c.1068G= (p.Thr356=)
c.861G= (p.Thr287=)
8g.144414268C>GCA463449575SLC39A4c.1143G>C (p.Thr381=)
c.1068G>C (p.Thr356=)
c.861G>C (p.Thr287=)
8g.144414268C>TCA4941387SLC39A4c.1143G>A (p.Thr381=)
c.1068G>A (p.Thr356=)
c.861G>A (p.Thr287=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
8g.144414269G>ACA4941388SLC39A4c.1142C>T (p.Thr381Met)
c.1067C>T (p.Thr356Met)
c.860C>T (p.Thr287Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414269G>CCA372621090SLC39A4c.1142C>G (p.Thr381Arg)
c.1067C>G (p.Thr356Arg)
c.860C>G (p.Thr287Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414269G=CA1826307059SLC39A4c.1142C= (p.Thr381=)
c.1067C= (p.Thr356=)
c.860C= (p.Thr287=)
8g.144414269G>TCA372621091SLC39A4c.1142C>A (p.Thr381Lys)
c.1067C>A (p.Thr356Lys)
c.860C>A (p.Thr287Lys)
8g.144414270T>ACA372621092SLC39A4c.1141A>T (p.Thr381Ser)
c.1066A>T (p.Thr356Ser)
c.859A>T (p.Thr287Ser)
8g.144414270T>CCA4941389SLC39A4c.1141A>G (p.Thr381Ala)
c.1066A>G (p.Thr356Ala)
c.859A>G (p.Thr287Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414270T>GCA372621093SLC39A4c.1141A>C (p.Thr381Pro)
c.1066A>C (p.Thr356Pro)
c.859A>C (p.Thr287Pro)
8g.144414270T=CA1826307060SLC39A4c.1141A= (p.Thr381=)
c.1066A= (p.Thr356=)
c.859A= (p.Thr287=)
8g.144414271C>ACA463449579SLC39A4c.1140G>T (p.Leu380=)
c.1065G>T (p.Leu355=)
c.858G>T (p.Leu286=)
 ClinVar gnomAD v4
8g.144414271C=CA1826307061SLC39A4c.1140G= (p.Leu380=)
c.1065G= (p.Leu355=)
c.858G= (p.Leu286=)
8g.144414271C>GCA463449581SLC39A4c.1140G>C (p.Leu380=)
c.1065G>C (p.Leu355=)
c.858G>C (p.Leu286=)
8g.144414271C>TCA463449580SLC39A4c.1140G>A (p.Leu380=)
c.1065G>A (p.Leu355=)
c.858G>A (p.Leu286=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
8g.144414274_144414284dupCA2695210376SLC39A4c.1130_1140dup (p.Thr381SerfsTer4)
c.1055_1065dup (p.Thr356SerfsTer4)
c.848_858dup (p.Thr287SerfsTer4)
8g.144414272A>CCA372621096SLC39A4c.1139T>G (p.Leu380Arg)
c.1064T>G (p.Leu355Arg)
c.857T>G (p.Leu286Arg)
8g.144414272A>GCA372621095SLC39A4c.1139T>C (p.Leu380Pro)
c.1064T>C (p.Leu355Pro)
c.857T>C (p.Leu286Pro)
8g.144414272A>TCA372621094SLC39A4c.1139T>A (p.Leu380Gln)
c.1064T>A (p.Leu355Gln)
c.857T>A (p.Leu286Gln)
8g.144414273G>ACA463449582SLC39A4c.1138C>T (p.Leu380=)
c.1063C>T (p.Leu355=)
c.856C>T (p.Leu286=)
 dbSNP gnomAD v2 gnomAD v4
8g.144414273G>CCA372621097SLC39A4c.1138C>G (p.Leu380Val)
c.1063C>G (p.Leu355Val)
c.856C>G (p.Leu286Val)
8g.144414273G=CA1826307062SLC39A4c.1138C= (p.Leu380=)
c.1063C= (p.Leu355=)
c.856C= (p.Leu286=)
8g.144414273G>TCA372621098SLC39A4c.1138C>A (p.Leu380Met)
c.1063C>A (p.Leu355Met)
c.856C>A (p.Leu286Met)
8g.144414274A>CCA372621099SLC39A4c.1137T>G (p.His379Gln)
c.1062T>G (p.His354Gln)
c.855T>G (p.His285Gln)
8g.144414274A>GCA463449583SLC39A4c.1137T>C (p.His379=)
c.1062T>C (p.His354=)
c.855T>C (p.His285=)
8g.144414274A>TCA372621100SLC39A4c.1137T>A (p.His379Gln)
c.1062T>A (p.His354Gln)
c.855T>A (p.His285Gln)
8g.144414275T>ACA372621101SLC39A4c.1136A>T (p.His379Leu)
c.1061A>T (p.His354Leu)
c.854A>T (p.His285Leu)
8g.144414275T>CCA372621102SLC39A4c.1136A>G (p.His379Arg)
c.1061A>G (p.His354Arg)
c.854A>G (p.His285Arg)
8g.144414275T>GCA372621103SLC39A4c.1136A>C (p.His379Pro)
c.1061A>C (p.His354Pro)
c.854A>C (p.His285Pro)
 gnomAD v4
8g.144414276G>ACA187648054SLC39A4c.1135C>T (p.His379Tyr)
c.1060C>T (p.His354Tyr)
c.853C>T (p.His285Tyr)
 dbSNP gnomAD v4
8g.144414276G>CCA372621104SLC39A4c.1135C>G (p.His379Asp)
c.1060C>G (p.His354Asp)
c.853C>G (p.His285Asp)
8g.144414276G=CA1826307063SLC39A4c.1135C= (p.His379=)
c.1060C= (p.His354=)
c.853C= (p.His285=)
8g.144414276G>TCA372621105SLC39A4c.1135C>A (p.His379Asn)
c.1060C>A (p.His354Asn)
c.853C>A (p.His285Asn)
8g.144414277C>ACA463449584SLC39A4c.1134G>T (p.Leu378=)
c.1059G>T (p.Leu353=)
c.852G>T (p.Leu284=)
 gnomAD v4
8g.144414277C=CA1826307064SLC39A4c.1134G= (p.Leu378=)
c.1059G= (p.Leu353=)
c.852G= (p.Leu284=)
8g.144414277C>GCA463449585SLC39A4c.1134G>C (p.Leu378=)
c.1059G>C (p.Leu353=)
c.852G>C (p.Leu284=)
8g.144414277C>TCA463449587SLC39A4c.1134G>A (p.Leu378=)
c.1059G>A (p.Leu353=)
c.852G>A (p.Leu284=)
 dbSNP gnomAD v2 gnomAD v4
8g.144414278A=CA1826307065SLC39A4c.1133T= (p.Leu378=)
c.1058T= (p.Leu353=)
c.851T= (p.Leu284=)
8g.144414278A>CCA372621106SLC39A4c.1133T>G (p.Leu378Arg)
c.1058T>G (p.Leu353Arg)
c.851T>G (p.Leu284Arg)
8g.144414278A>GCA372621107SLC39A4c.1133T>C (p.Leu378Pro)
c.1058T>C (p.Leu353Pro)
c.851T>C (p.Leu284Pro)
 dbSNP gnomAD v2 gnomAD v4
8g.144414278A>TCA372621108SLC39A4c.1133T>A (p.Leu378Gln)
c.1058T>A (p.Leu353Gln)
c.851T>A (p.Leu284Gln)
8g.144414279G>ACA463449590SLC39A4c.1132C>T (p.Leu378=)
c.1057C>T (p.Leu353=)
c.850C>T (p.Leu284=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.144414279G>CCA372621110SLC39A4c.1132C>G (p.Leu378Val)
c.1057C>G (p.Leu353Val)
c.850C>G (p.Leu284Val)
8g.144414279G=CA1826307066SLC39A4c.1132C= (p.Leu378=)
c.1057C= (p.Leu353=)
c.850C= (p.Leu284=)
8g.144414279G>TCA372621109SLC39A4c.1132C>A (p.Leu378Met)
c.1057C>A (p.Leu353Met)
c.850C>A (p.Leu284Met)
 gnomAD v4
8g.144414280delCA2573143007SLC39A4c.1132del (p.Leu378CysfsTer3)
c.1057del (p.Leu353CysfsTer3)
c.850del (p.Leu284CysfsTer3)
 ClinVar dbSNP gnomAD v4
8g.144414280G>ACA463449591SLC39A4c.1131C>T (p.Val377=)
c.1056C>T (p.Val352=)
c.849C>T (p.Val283=)
 dbSNP gnomAD v4
8g.144414280G>CCA4941390SLC39A4c.1131C>G (p.Val377=)
c.1056C>G (p.Val352=)
c.849C>G (p.Val283=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414280G=CA1826307067SLC39A4c.1131C= (p.Val377=)
c.1056C= (p.Val352=)
c.849C= (p.Val283=)
8g.144414280G>TCA463449592SLC39A4c.1131C>A (p.Val377=)
c.1056C>A (p.Val352=)
c.849C>A (p.Val283=)
8g.144414281A>CCA372621111SLC39A4c.1130T>G (p.Val377Gly)
c.1055T>G (p.Val352Gly)
c.848T>G (p.Val283Gly)
8g.144414281A>GCA372621112SLC39A4c.1130T>C (p.Val377Ala)
c.1055T>C (p.Val352Ala)
c.848T>C (p.Val283Ala)
8g.144414281A>TCA372621113SLC39A4c.1130T>A (p.Val377Asp)
c.1055T>A (p.Val352Asp)
c.848T>A (p.Val283Asp)
8g.144414282C>ACA372621114SLC39A4c.1129G>T (p.Val377Phe)
c.1054G>T (p.Val352Phe)
c.847G>T (p.Val283Phe)
 gnomAD v4
8g.144414282C>GCA372621115SLC39A4c.1129G>C (p.Val377Leu)
c.1054G>C (p.Val352Leu)
c.847G>C (p.Val283Leu)
8g.144414282C>TCA372621116SLC39A4c.1129G>A (p.Val377Ile)
c.1054G>A (p.Val352Ile)
c.847G>A (p.Val283Ile)
 gnomAD v4
8g.144414283A>CCA463449594SLC39A4c.1128T>G (p.Ala376=)
c.1053T>G (p.Ala351=)
c.846T>G (p.Ala282=)
 ClinVar dbSNP
8g.144414283A>GCA463449595SLC39A4c.1128T>C (p.Ala376=)
c.1053T>C (p.Ala351=)
c.846T>C (p.Ala282=)
8g.144414283A>TCA463449596SLC39A4c.1128T>A (p.Ala376=)
c.1053T>A (p.Ala351=)
c.846T>A (p.Ala282=)
8g.144414284G>ACA372621117SLC39A4c.1127C>T (p.Ala376Val)
c.1052C>T (p.Ala351Val)
c.845C>T (p.Ala282Val)
 gnomAD v4
8g.144414284G>CCA372621118SLC39A4c.1127C>G (p.Ala376Gly)
c.1052C>G (p.Ala351Gly)
c.845C>G (p.Ala282Gly)
8g.144414284G>TCA372621119SLC39A4c.1127C>A (p.Ala376Asp)
c.1052C>A (p.Ala351Asp)
c.845C>A (p.Ala282Asp)
8g.144414285C>ACA4941392SLC39A4c.1126G>T (p.Ala376Ser)
c.1051G>T (p.Ala351Ser)
c.844G>T (p.Ala282Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414285C=CA1826307068SLC39A4c.1126G= (p.Ala376=)
c.1051G= (p.Ala351=)
c.844G= (p.Ala282=)
8g.144414285C>GCA372621120SLC39A4c.1126G>C (p.Ala376Pro)
c.1051G>C (p.Ala351Pro)
c.844G>C (p.Ala282Pro)
8g.144414285C>TCA4941391SLC39A4c.1126G>A (p.Ala376Thr)
c.1051G>A (p.Ala351Thr)
c.844G>A (p.Ala282Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414286G>ACA4941393SLC39A4c.1125C>T (p.Asp375=)
c.1050C>T (p.Asp350=)
c.843C>T (p.Asp281=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414286G>CCA372621122SLC39A4c.1125C>G (p.Asp375Glu)
c.1050C>G (p.Asp350Glu)
c.843C>G (p.Asp281Glu)
8g.144414286G=CA1826307069SLC39A4c.1125C= (p.Asp375=)
c.1050C= (p.Asp350=)
c.843C= (p.Asp281=)
8g.144414286G>TCA372621121SLC39A4c.1125C>A (p.Asp375Glu)
c.1050C>A (p.Asp350Glu)
c.843C>A (p.Asp281Glu)
8g.144414287T>ACA372621125SLC39A4c.1124A>T (p.Asp375Val)
c.1049A>T (p.Asp350Val)
c.842A>T (p.Asp281Val)
8g.144414287T>CCA372621123SLC39A4c.1124A>G (p.Asp375Gly)
c.1049A>G (p.Asp350Gly)
c.842A>G (p.Asp281Gly)
 dbSNP gnomAD v2 gnomAD v4
8g.144414287T>GCA372621124SLC39A4c.1124A>C (p.Asp375Ala)
c.1049A>C (p.Asp350Ala)
c.842A>C (p.Asp281Ala)
8g.144414287T=CA1826307070SLC39A4c.1124A= (p.Asp375=)
c.1049A= (p.Asp350=)
c.842A= (p.Asp281=)
8g.144414288C>ACA372621126SLC39A4c.1123G>T (p.Asp375Tyr)
c.1048G>T (p.Asp350Tyr)
c.841G>T (p.Asp281Tyr)
 dbSNP gnomAD v2
8g.144414288C=CA1826307071SLC39A4c.1123G= (p.Asp375=)
c.1048G= (p.Asp350=)
c.841G= (p.Asp281=)
8g.144414288C>GCA4941395SLC39A4c.1123G>C (p.Asp375His)
c.1048G>C (p.Asp350His)
c.841G>C (p.Asp281His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414288C>TCA4941394SLC39A4c.1123G>A (p.Asp375Asn)
c.1048G>A (p.Asp350Asn)
c.841G>A (p.Asp281Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414291delCA2689098465SLC39A4c.1123del (p.Asp375ThrfsTer6)
c.1048del (p.Asp350ThrfsTer6)
c.841del (p.Asp281ThrfsTer6)
 gnomAD v4
8g.144414289C>ACA463449600SLC39A4c.1122G>T (p.Gly374=)
c.1047G>T (p.Gly349=)
c.840G>T (p.Gly280=)
8g.144414289C=CA1826307072SLC39A4c.1122G= (p.Gly374=)
c.1047G= (p.Gly349=)
c.840G= (p.Gly280=)
8g.144414289C>GCA4941397SLC39A4c.1122G>C (p.Gly374=)
c.1047G>C (p.Gly349=)
c.840G>C (p.Gly280=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144414289C>TCA4941396SLC39A4c.1122G>A (p.Gly374=)
c.1047G>A (p.Gly349=)
c.840G>A (p.Gly280=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.144414290C>ACA372621127SLC39A4c.1121G>T (p.Gly374Val)
c.1046G>T (p.Gly349Val)
c.839G>T (p.Gly280Val)
 dbSNP gnomAD v2 gnomAD v4
8g.144414290C=CA1826307073SLC39A4c.1121G= (p.Gly374=)
c.1046G= (p.Gly349=)
c.839G= (p.Gly280=)
8g.144414290C>GCA372621128SLC39A4c.1121G>C (p.Gly374Ala)
c.1046G>C (p.Gly349Ala)
c.839G>C (p.Gly280Ala)
 dbSNP
8g.144414290C>TCA372621129SLC39A4c.1121G>A (p.Gly374Glu)
c.1046G>A (p.Gly349Glu)
c.839G>A (p.Gly280Glu)
 dbSNP gnomAD v2 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)

Number of alleles fetched