Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.144413406_144414398del | CA2580078692 | SLC39A4 | c.1023_1475-7del c.948_1400-7del c.1023_1474+117del c.741_1193-7del c.741_1192+117del | ClinVar |
8 | g.144414311A>C | CA372621165 | SLC39A4 | c.1100T>G (p.Leu367Arg) c.1025T>G (p.Leu342Arg) c.818T>G (p.Leu273Arg) | |
8 | g.144414311A>G | CA372621166 | SLC39A4 | c.1100T>C (p.Leu367Pro) c.1025T>C (p.Leu342Pro) c.818T>C (p.Leu273Pro) | |
8 | g.144414311A>T | CA372621167 | SLC39A4 | c.1100T>A (p.Leu367Gln) c.1025T>A (p.Leu342Gln) c.818T>A (p.Leu273Gln) | |
8 | g.144414312G>A | CA463449625 | SLC39A4 | c.1099C>T (p.Leu367=) c.1024C>T (p.Leu342=) c.817C>T (p.Leu273=) | |
8 | g.144414312G>C | CA372621168 | SLC39A4 | c.1099C>G (p.Leu367Val) c.1024C>G (p.Leu342Val) c.817C>G (p.Leu273Val) | |
8 | g.144414312G>T | CA372621169 | SLC39A4 | c.1099C>A (p.Leu367Met) c.1024C>A (p.Leu342Met) c.817C>A (p.Leu273Met) | |
8 | g.144414313G>A | CA463449626 | SLC39A4 | c.1098C>T (p.Ser366=) c.1023C>T (p.Ser341=) c.816C>T (p.Ser272=) | gnomAD v4 |
8 | g.144414313G>C | CA372621170 | SLC39A4 | c.1098C>G (p.Ser366Arg) c.1023C>G (p.Ser341Arg) c.816C>G (p.Ser272Arg) | gnomAD v4 |
8 | g.144414313G>T | CA372621171 | SLC39A4 | c.1098C>A (p.Ser366Arg) c.1023C>A (p.Ser341Arg) c.816C>A (p.Ser272Arg) | COSMIC COSMIC |
8 | g.144414314C>A | CA372621173 | SLC39A4 | c.1097G>T (p.Ser366Ile) c.1022G>T (p.Ser341Ile) c.815G>T (p.Ser272Ile) | |
8 | g.144414314C= | CA1826307085 | SLC39A4 | c.1097G= (p.Ser366=) c.1022G= (p.Ser341=) c.815G= (p.Ser272=) | |
8 | g.144414314C>G | CA372621174 | SLC39A4 | c.1097G>C (p.Ser366Thr) c.1022G>C (p.Ser341Thr) c.815G>C (p.Ser272Thr) | |
8 | g.144414314C>T | CA372621172 | SLC39A4 | c.1097G>A (p.Ser366Asn) c.1022G>A (p.Ser341Asn) c.815G>A (p.Ser272Asn) | dbSNP gnomAD v4 |
8 | g.144414315T>A | CA372621175 | SLC39A4 | c.1096A>T (p.Ser366Cys) c.1021A>T (p.Ser341Cys) c.814A>T (p.Ser272Cys) | |
8 | g.144414315T>C | CA372621176 | SLC39A4 | c.1096A>G (p.Ser366Gly) c.1021A>G (p.Ser341Gly) c.814A>G (p.Ser272Gly) | |
8 | g.144414315T>G | CA372621177 | SLC39A4 | c.1096A>C (p.Ser366Arg) c.1021A>C (p.Ser341Arg) c.814A>C (p.Ser272Arg) | |
8 | g.144414316C>A | CA463449631 | SLC39A4 | c.1095G>T (p.Leu365=) c.1020G>T (p.Leu340=) c.813G>T (p.Leu271=) | |
8 | g.144414316C>G | CA463449632 | SLC39A4 | c.1095G>C (p.Leu365=) c.1020G>C (p.Leu340=) c.813G>C (p.Leu271=) | |
8 | g.144414316C>T | CA463449633 | SLC39A4 | c.1095G>A (p.Leu365=) c.1020G>A (p.Leu340=) c.813G>A (p.Leu271=) | gnomAD v4 |
8 | g.144414321_144414332del | CA2689098548 | SLC39A4 | c.1084_1095del (p.Gln362_Leu365del) c.1009_1020del (p.Gln337_Leu340del) c.802_813del (p.Gln268_Leu271del) | gnomAD v4 |
8 | g.144414317A>C | CA372621178 | SLC39A4 | c.1094T>G (p.Leu365Arg) c.1019T>G (p.Leu340Arg) c.812T>G (p.Leu271Arg) | |
8 | g.144414317A>G | CA372621179 | SLC39A4 | c.1094T>C (p.Leu365Pro) c.1019T>C (p.Leu340Pro) c.812T>C (p.Leu271Pro) | gnomAD v4 |
8 | g.144414317A>T | CA372621180 | SLC39A4 | c.1094T>A (p.Leu365Gln) c.1019T>A (p.Leu340Gln) c.812T>A (p.Leu271Gln) | |
8 | g.144414318G>A | CA463449634 | SLC39A4 | c.1093C>T (p.Leu365=) c.1018C>T (p.Leu340=) c.811C>T (p.Leu271=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414318G>C | CA372621181 | SLC39A4 | c.1093C>G (p.Leu365Val) c.1018C>G (p.Leu340Val) c.811C>G (p.Leu271Val) | |
8 | g.144414318G= | CA1826307086 | SLC39A4 | c.1093C= (p.Leu365=) c.1018C= (p.Leu340=) c.811C= (p.Leu271=) | |
8 | g.144414318G>T | CA372621182 | SLC39A4 | c.1093C>A (p.Leu365Met) c.1018C>A (p.Leu340Met) c.811C>A (p.Leu271Met) | gnomAD v4 |
8 | g.144414319G>A | CA463449635 | SLC39A4 | c.1092C>T (p.Phe364=) c.1017C>T (p.Phe339=) c.810C>T (p.Phe270=) | |
8 | g.144414319G>C | CA372621183 | SLC39A4 | c.1092C>G (p.Phe364Leu) c.1017C>G (p.Phe339Leu) c.810C>G (p.Phe270Leu) | |
8 | g.144414319G>T | CA372621184 | SLC39A4 | c.1092C>A (p.Phe364Leu) c.1017C>A (p.Phe339Leu) c.810C>A (p.Phe270Leu) | |
8 | g.144414320A>C | CA372621185 | SLC39A4 | c.1091T>G (p.Phe364Cys) c.1016T>G (p.Phe339Cys) c.809T>G (p.Phe270Cys) | |
8 | g.144414320A>G | CA372621186 | SLC39A4 | c.1091T>C (p.Phe364Ser) c.1016T>C (p.Phe339Ser) c.809T>C (p.Phe270Ser) | |
8 | g.144414320A>T | CA372621187 | SLC39A4 | c.1091T>A (p.Phe364Tyr) c.1016T>A (p.Phe339Tyr) c.809T>A (p.Phe270Tyr) | |
8 | g.144414321A= | CA1826307087 | SLC39A4 | c.1090T= (p.Phe364=) c.1015T= (p.Phe339=) c.808T= (p.Phe270=) | |
8 | g.144414321A>C | CA372621190 | SLC39A4 | c.1090T>G (p.Phe364Val) c.1015T>G (p.Phe339Val) c.808T>G (p.Phe270Val) | |
8 | g.144414321A>G | CA372621189 | SLC39A4 | c.1090T>C (p.Phe364Leu) c.1015T>C (p.Phe339Leu) c.808T>C (p.Phe270Leu) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414321A>T | CA372621188 | SLC39A4 | c.1090T>A (p.Phe364Ile) c.1015T>A (p.Phe339Ile) c.808T>A (p.Phe270Ile) | |
8 | g.144414322G>A | CA4941404 | SLC39A4 | c.1089C>T (p.Thr363=) c.1014C>T (p.Thr338=) c.807C>T (p.Thr269=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.144414322G>C | CA463449640 | SLC39A4 | c.1089C>G (p.Thr363=) c.1014C>G (p.Thr338=) c.807C>G (p.Thr269=) | |
8 | g.144414322G= | CA1826307088 | SLC39A4 | c.1089C= (p.Thr363=) c.1014C= (p.Thr338=) c.807C= (p.Thr269=) | |
8 | g.144414322G>T | CA463449639 | SLC39A4 | c.1089C>A (p.Thr363=) c.1014C>A (p.Thr338=) c.807C>A (p.Thr269=) | gnomAD v4 |
8 | g.144414323dup | CA1139660828 | SLC39A4 | c.1089dup (p.Phe364LeufsTer?) c.1014dup (p.Phe339LeufsTer?) c.807dup (p.Phe270LeufsTer?) | ClinVar dbSNP |
8 | g.144414323G>A | CA372621191 | SLC39A4 | c.1088C>T (p.Thr363Ile) c.1013C>T (p.Thr338Ile) c.806C>T (p.Thr269Ile) | dbSNP |
8 | g.144414323G>C | CA372621192 | SLC39A4 | c.1088C>G (p.Thr363Ser) c.1013C>G (p.Thr338Ser) c.806C>G (p.Thr269Ser) | dbSNP gnomAD v4 |
8 | g.144414323G= | CA1826307089 | SLC39A4 | c.1088C= (p.Thr363=) c.1013C= (p.Thr338=) c.806C= (p.Thr269=) | |
8 | g.144414323G>T | CA372621193 | SLC39A4 | c.1088C>A (p.Thr363Asn) c.1013C>A (p.Thr338Asn) c.806C>A (p.Thr269Asn) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414324T>A | CA372621194 | SLC39A4 | c.1087A>T (p.Thr363Ser) c.1012A>T (p.Thr338Ser) c.805A>T (p.Thr269Ser) | gnomAD v4 |
8 | g.144414324T>C | CA372621195 | SLC39A4 | c.1087A>G (p.Thr363Ala) c.1012A>G (p.Thr338Ala) c.805A>G (p.Thr269Ala) | |
8 | g.144414324T>G | CA372621196 | SLC39A4 | c.1087A>C (p.Thr363Pro) c.1012A>C (p.Thr338Pro) c.805A>C (p.Thr269Pro) | |
8 | g.144414325C>A | CA372621197 | SLC39A4 | c.1086G>T (p.Gln362His) c.1011G>T (p.Gln337His) c.804G>T (p.Gln268His) | gnomAD v4 |
8 | g.144414325C>G | CA372621198 | SLC39A4 | c.1086G>C (p.Gln362His) c.1011G>C (p.Gln337His) c.804G>C (p.Gln268His) | |
8 | g.144414325C>T | CA463449641 | SLC39A4 | c.1086G>A (p.Gln362=) c.1011G>A (p.Gln337=) c.804G>A (p.Gln268=) | gnomAD v4 |
8 | g.144414326T>A | CA372621199 | SLC39A4 | c.1085A>T (p.Gln362Leu) c.1010A>T (p.Gln337Leu) c.803A>T (p.Gln268Leu) | |
8 | g.144414326T>C | CA372621200 | SLC39A4 | c.1085A>G (p.Gln362Arg) c.1010A>G (p.Gln337Arg) c.803A>G (p.Gln268Arg) | gnomAD v4 |
8 | g.144414326T>G | CA372621201 | SLC39A4 | c.1085A>C (p.Gln362Pro) c.1010A>C (p.Gln337Pro) c.803A>C (p.Gln268Pro) | |
8 | g.144414327G>A | CA372621202 | SLC39A4 | c.1084C>T (p.Gln362Ter) c.1009C>T (p.Gln337Ter) c.802C>T (p.Gln268Ter) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414327G>C | CA372621203 | SLC39A4 | c.1084C>G (p.Gln362Glu) c.1009C>G (p.Gln337Glu) c.802C>G (p.Gln268Glu) | |
8 | g.144414327G= | CA1826307090 | SLC39A4 | c.1084C= (p.Gln362=) c.1009C= (p.Gln337=) c.802C= (p.Gln268=) | |
8 | g.144414327G>T | CA372621204 | SLC39A4 | c.1084C>A (p.Gln362Lys) c.1009C>A (p.Gln337Lys) c.802C>A (p.Gln268Lys) | |
8 | g.144414328C>A | CA463449642 | SLC39A4 | c.1083G>T (p.Leu361=) c.1008G>T (p.Leu336=) c.801G>T (p.Leu267=) | gnomAD v4 |
8 | g.144414328C>G | CA463449643 | SLC39A4 | c.1083G>C (p.Leu361=) c.1008G>C (p.Leu336=) c.801G>C (p.Leu267=) | |
8 | g.144414328C>T | CA463449644 | SLC39A4 | c.1083G>A (p.Leu361=) c.1008G>A (p.Leu336=) c.801G>A (p.Leu267=) | gnomAD v4 |
8 | g.144414329A>C | CA372621206 | SLC39A4 | c.1082T>G (p.Leu361Arg) c.1007T>G (p.Leu336Arg) c.800T>G (p.Leu267Arg) | |
8 | g.144414329A>G | CA372621207 | SLC39A4 | c.1082T>C (p.Leu361Pro) c.1007T>C (p.Leu336Pro) c.800T>C (p.Leu267Pro) | gnomAD v4 |
8 | g.144414329A>T | CA372621205 | SLC39A4 | c.1082T>A (p.Leu361Gln) c.1007T>A (p.Leu336Gln) c.800T>A (p.Leu267Gln) | gnomAD v4 |
8 | g.144414330G>A | CA463449648 | SLC39A4 | c.1081C>T (p.Leu361=) c.1006C>T (p.Leu336=) c.799C>T (p.Leu267=) | dbSNP gnomAD v4 |
8 | g.144414330G>C | CA372621208 | SLC39A4 | c.1081C>G (p.Leu361Val) c.1006C>G (p.Leu336Val) c.799C>G (p.Leu267Val) | |
8 | g.144414330G= | CA1826307091 | SLC39A4 | c.1081C= (p.Leu361=) c.1006C= (p.Leu336=) c.799C= (p.Leu267=) | |
8 | g.144414330G>T | CA372621209 | SLC39A4 | c.1081C>A (p.Leu361Met) c.1006C>A (p.Leu336Met) c.799C>A (p.Leu267Met) | gnomAD v4 |
8 | g.144414331G>A | CA463449650 | SLC39A4 | c.1080C>T (p.Ile360=) c.1005C>T (p.Ile335=) c.798C>T (p.Ile266=) | ClinVar dbSNP gnomAD v2 |
8 | g.144414331G>C | CA4941405 | SLC39A4 | c.1080C>G (p.Ile360Met) c.1005C>G (p.Ile335Met) c.798C>G (p.Ile266Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.144414331G= | CA1826307092 | SLC39A4 | c.1080C= (p.Ile360=) c.1005C= (p.Ile335=) c.798C= (p.Ile266=) | |
8 | g.144414331G>T | CA463449649 | SLC39A4 | c.1080C>A (p.Ile360=) c.1005C>A (p.Ile335=) c.798C>A (p.Ile266=) | |
8 | g.144414332A= | CA1826307093 | SLC39A4 | c.1079T= (p.Ile360=) c.1004T= (p.Ile335=) c.797T= (p.Ile266=) | |
8 | g.144414332A>C | CA372621210 | SLC39A4 | c.1079T>G (p.Ile360Ser) c.1004T>G (p.Ile335Ser) c.797T>G (p.Ile266Ser) | |
8 | g.144414332A>G | CA372621211 | SLC39A4 | c.1079T>C (p.Ile360Thr) c.1004T>C (p.Ile335Thr) c.797T>C (p.Ile266Thr) | gnomAD v4 |
8 | g.144414332A>T | CA4941406 | SLC39A4 | c.1079T>A (p.Ile360Asn) c.1004T>A (p.Ile335Asn) c.797T>A (p.Ile266Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.144414333T>A | CA372621214 | SLC39A4 | c.1078A>T (p.Ile360Phe) c.1003A>T (p.Ile335Phe) c.796A>T (p.Ile266Phe) | gnomAD v4 |
8 | g.144414333T>C | CA372621212 | SLC39A4 | c.1078A>G (p.Ile360Val) c.1003A>G (p.Ile335Val) c.796A>G (p.Ile266Val) | dbSNP gnomAD v4 |
8 | g.144414333T>G | CA372621213 | SLC39A4 | c.1078A>C (p.Ile360Leu) c.1003A>C (p.Ile335Leu) c.796A>C (p.Ile266Leu) | |
8 | g.144414333T= | CA1826307094 | SLC39A4 | c.1078A= (p.Ile360=) c.1003A= (p.Ile335=) c.796A= (p.Ile266=) | |
8 | g.144414334G>A | CA463449651 | SLC39A4 | c.1077C>T (p.Tyr359=) c.1002C>T (p.Tyr334=) c.795C>T (p.Tyr265=) | ClinVar dbSNP gnomAD v4 |
8 | g.144414334G>C | CA372621215 | SLC39A4 | c.1077C>G (p.Tyr359Ter) c.1002C>G (p.Tyr334Ter) c.795C>G (p.Tyr265Ter) | |
8 | g.144414334G= | CA1826307095 | SLC39A4 | c.1077C= (p.Tyr359=) c.1002C= (p.Tyr334=) c.795C= (p.Tyr265=) | |
8 | g.144414334G>T | CA372621216 | SLC39A4 | c.1077C>A (p.Tyr359Ter) c.1002C>A (p.Tyr334Ter) c.795C>A (p.Tyr265Ter) | gnomAD v4 |
8 | g.144414335T>A | CA372621217 | SLC39A4 | c.1076A>T (p.Tyr359Phe) c.1001A>T (p.Tyr334Phe) c.794A>T (p.Tyr265Phe) | |
8 | g.144414335T>C | CA372621218 | SLC39A4 | c.1076A>G (p.Tyr359Cys) c.1001A>G (p.Tyr334Cys) c.794A>G (p.Tyr265Cys) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414335T>G | CA372621219 | SLC39A4 | c.1076A>C (p.Tyr359Ser) c.1001A>C (p.Tyr334Ser) c.794A>C (p.Tyr265Ser) | |
8 | g.144414335T= | CA1826307096 | SLC39A4 | c.1076A= (p.Tyr359=) c.1001A= (p.Tyr334=) c.794A= (p.Tyr265=) | |
8 | g.144414336A>C | CA372621220 | SLC39A4 | c.1075T>G (p.Tyr359Asp) c.1000T>G (p.Tyr334Asp) c.793T>G (p.Tyr265Asp) | |
8 | g.144414336A>G | CA372621222 | SLC39A4 | c.1075T>C (p.Tyr359His) c.1000T>C (p.Tyr334His) c.793T>C (p.Tyr265His) | |
8 | g.144414336A>T | CA372621221 | SLC39A4 | c.1075T>A (p.Tyr359Asn) c.1000T>A (p.Tyr334Asn) c.793T>A (p.Tyr265Asn) | |
8 | g.144414337G>A | CA4941407 | SLC39A4 | c.1074C>T (p.His358=) c.999C>T (p.His333=) c.792C>T (p.His264=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.144414337G>C | CA372621223 | SLC39A4 | c.1074C>G (p.His358Gln) c.999C>G (p.His333Gln) c.792C>G (p.His264Gln) | |
8 | g.144414337G= | CA1826307097 | SLC39A4 | c.1074C= (p.His358=) c.999C= (p.His333=) c.792C= (p.His264=) | |
8 | g.144414337G>T | CA372621224 | SLC39A4 | c.1074C>A (p.His358Gln) c.999C>A (p.His333Gln) c.792C>A (p.His264Gln) | |
8 | g.144414338T>A | CA372621225 | SLC39A4 | c.1073A>T (p.His358Leu) c.998A>T (p.His333Leu) c.791A>T (p.His264Leu) | |
8 | g.144414338T>C | CA372621226 | SLC39A4 | c.1073A>G (p.His358Arg) c.998A>G (p.His333Arg) c.791A>G (p.His264Arg) | dbSNP gnomAD v4 |
8 | g.144414338T>G | CA372621227 | SLC39A4 | c.1073A>C (p.His358Pro) c.998A>C (p.His333Pro) c.791A>C (p.His264Pro) | |
8 | g.144414338T= | CA1826307098 | SLC39A4 | c.1073A= (p.His358=) c.998A= (p.His333=) c.791A= (p.His264=) | |
8 | g.144414339G>A | CA372621228 | SLC39A4 | c.1072C>T (p.His358Tyr) c.997C>T (p.His333Tyr) c.790C>T (p.His264Tyr) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414339G>C | CA372621229 | SLC39A4 | c.1072C>G (p.His358Asp) c.997C>G (p.His333Asp) c.790C>G (p.His264Asp) | |
8 | g.144414339G= | CA1826307099 | SLC39A4 | c.1072C= (p.His358=) c.997C= (p.His333=) c.790C= (p.His264=) | |
8 | g.144414339G>T | CA372621230 | SLC39A4 | c.1072C>A (p.His358Asn) c.997C>A (p.His333Asn) c.790C>A (p.His264Asn) | |
8 | g.144414340G>A | CA463449655 | SLC39A4 | c.1071C>T (p.Thr357=) c.996C>T (p.Thr332=) c.789C>T (p.Thr263=) | dbSNP gnomAD v2 |
8 | g.144414340G>C | CA463449657 | SLC39A4 | c.1071C>G (p.Thr357=) c.996C>G (p.Thr332=) c.789C>G (p.Thr263=) | ClinVar gnomAD v4 |
8 | g.144414340G= | CA1826307100 | SLC39A4 | c.1071C= (p.Thr357=) c.996C= (p.Thr332=) c.789C= (p.Thr263=) | |
8 | g.144414340G>T | CA463449656 | SLC39A4 | c.1071C>A (p.Thr357=) c.996C>A (p.Thr332=) c.789C>A (p.Thr263=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414340_144414341insTA | CA2689098692 | SLC39A4 | c.1070_1071insTA (p.His358ThrfsTer9) c.995_996insTA (p.His333ThrfsTer9) c.788_789insTA (p.His264ThrfsTer9) | gnomAD v4 |
8 | g.144414341G>A | CA4941408 | SLC39A4 | c.1070C>T (p.Thr357Ile) c.995C>T (p.Thr332Ile) c.788C>T (p.Thr263Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414341G>C | CA372621231 | SLC39A4 | c.1070C>G (p.Thr357Ser) c.995C>G (p.Thr332Ser) c.788C>G (p.Thr263Ser) | |
8 | g.144414341G= | CA1826307101 | SLC39A4 | c.1070C= (p.Thr357=) c.995C= (p.Thr332=) c.788C= (p.Thr263=) | |
8 | g.144414341G>T | CA372621232 | SLC39A4 | c.1070C>A (p.Thr357Asn) c.995C>A (p.Thr332Asn) c.788C>A (p.Thr263Asn) | |
8 | g.144414342_144414394dup | CA2580078709 | SLC39A4 | c.1018_1070dup (p.His358AlafsTer9) c.943_995dup (p.His333AlafsTer9) c.736_788dup (p.His264AlafsTer9) | ClinVar dbSNP |
8 | g.144414342T>A | CA372621234 | SLC39A4 | c.1069A>T (p.Thr357Ser) c.994A>T (p.Thr332Ser) c.787A>T (p.Thr263Ser) | dbSNP gnomAD v4 |
8 | g.144414342T>C | CA4941409 | SLC39A4 | c.1069A>G (p.Thr357Ala) c.994A>G (p.Thr332Ala) c.787A>G (p.Thr263Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414342T>G | CA372621233 | SLC39A4 | c.1069A>C (p.Thr357Pro) c.994A>C (p.Thr332Pro) c.787A>C (p.Thr263Pro) | |
8 | g.144414342T= | CA1826307102 | SLC39A4 | c.1069A= (p.Thr357=) c.994A= (p.Thr332=) c.787A= (p.Thr263=) | |
8 | g.144414342_144414343delinsCA | CA2499219171 | SLC39A4 | c.1068_1069delinsTG (p.Thr357Ala) c.993_994delinsTG (p.Thr332Ala) c.786_787delinsTG (p.Thr263Ala) | ClinVar |
8 | g.144414343G>A | CA4941410 | SLC39A4 | c.1068C>T (p.Val356=) c.993C>T (p.Val331=) c.786C>T (p.Val262=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414343G>C | CA463449659 | SLC39A4 | c.1068C>G (p.Val356=) c.993C>G (p.Val331=) c.786C>G (p.Val262=) | |
8 | g.144414343G= | CA1826307103 | SLC39A4 | c.1068C= (p.Val356=) c.993C= (p.Val331=) c.786C= (p.Val262=) | |
8 | g.144414343G>T | CA463449660 | SLC39A4 | c.1068C>A (p.Val356=) c.993C>A (p.Val331=) c.786C>A (p.Val262=) | |
8 | g.144414343_144414344insGGCG | CA2689098723 | SLC39A4 | c.1068_1069insGCCC (p.Thr357AlafsTer?) c.993_994insGCCC (p.Thr332AlafsTer?) c.786_787insGCCC (p.Thr263AlafsTer?) | gnomAD v4 |
8 | g.144414376_144414377insGCCAGGCTCAGGAAGGTCTGCAGGATGTAGTGGGCGACCCCCCTGCAGCCAGTGCAGGTCAGCAGCAGG | CA2512985975 | SLC39A4 | c.1068_1069insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC (p.Val356_Thr357insAlaHisTyrIleLeuGlnThrPheLeuSerLeuAlaLeuLeuLeuThrCysThrGlyCysArgGlyVal) c.993_994insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC (p.Val331_Thr332insAlaHisTyrIleLeuGlnThrPheLeuSerLeuAlaLeuLeuLeuThrCysThrGlyCysArgGlyVal) c.786_787insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC (p.Val262_Thr263insAlaHisTyrIleLeuGlnThrPheLeuSerLeuAlaLeuLeuLeuThrCysThrGlyCysArgGlyVal) | |
8 | g.144414344A= | CA1826307105 | SLC39A4 | c.1067T= (p.Val356=) c.992T= (p.Val331=) c.785T= (p.Val262=) | |
8 | g.144414344A>C | CA4941411 | SLC39A4 | c.1067T>G (p.Val356Gly) c.992T>G (p.Val331Gly) c.785T>G (p.Val262Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.144414344A>G | CA372621236 | SLC39A4 | c.1067T>C (p.Val356Ala) c.992T>C (p.Val331Ala) c.785T>C (p.Val262Ala) | |
8 | g.144414344A>T | CA372621235 | SLC39A4 | c.1067T>A (p.Val356Asp) c.992T>A (p.Val331Asp) c.785T>A (p.Val262Asp) | |
8 | g.144414344_144414345delinsAC | CA1826307104 | SLC39A4 | c.1066_1067delinsGT (p.Val356=) c.991_992delinsGT (p.Val331=) c.784_785delinsGT (p.Val262=) | |
8 | g.144414345C>A | CA372621237 | SLC39A4 | c.1066G>T (p.Val356Phe) c.991G>T (p.Val331Phe) c.784G>T (p.Val262Phe) | ClinVar dbSNP gnomAD v4 |
8 | g.144414345C= | CA1826307106 | SLC39A4 | c.1066G= (p.Val356=) c.991G= (p.Val331=) c.784G= (p.Val262=) | |
8 | g.144414345C>G | CA372621238 | SLC39A4 | c.1066G>C (p.Val356Leu) c.991G>C (p.Val331Leu) c.784G>C (p.Val262Leu) | gnomAD v4 |
8 | g.144414345C>T | CA4941413 | SLC39A4 | c.1066G>A (p.Val356Ile) c.991G>A (p.Val331Ile) c.784G>A (p.Val262Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414350dup | CA4941412 | SLC39A4 | c.1066dup (p.Val356GlyfsTer?) c.991dup (p.Val331GlyfsTer?) c.784dup (p.Val262GlyfsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.144414350del | CA586164241 | SLC39A4 | c.1066del (p.Val356SerfsTer10) c.991del (p.Val331SerfsTer10) c.784del (p.Val262SerfsTer10) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
8 | g.144414346C>A | CA463449661 | SLC39A4 | c.1065G>T (p.Gly355=) c.990G>T (p.Gly330=) c.783G>T (p.Gly261=) | gnomAD v4 |
8 | g.144414346C= | CA1826307107 | SLC39A4 | c.1065G= (p.Gly355=) c.990G= (p.Gly330=) c.783G= (p.Gly261=) | |
8 | g.144414346C>G | CA463449663 | SLC39A4 | c.1065G>C (p.Gly355=) c.990G>C (p.Gly330=) c.783G>C (p.Gly261=) | dbSNP |
8 | g.144414346C>T | CA463449665 | SLC39A4 | c.1065G>A (p.Gly355=) c.990G>A (p.Gly330=) c.783G>A (p.Gly261=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414347C>A | CA187648236 | SLC39A4 | c.1064G>T (p.Gly355Val) c.989G>T (p.Gly330Val) c.782G>T (p.Gly261Val) | dbSNP gnomAD v4 |
8 | g.144414347C= | CA1826307108 | SLC39A4 | c.1064G= (p.Gly355=) c.989G= (p.Gly330=) c.782G= (p.Gly261=) | |
8 | g.144414347C>G | CA372621239 | SLC39A4 | c.1064G>C (p.Gly355Ala) c.989G>C (p.Gly330Ala) c.782G>C (p.Gly261Ala) | gnomAD v4 |
8 | g.144414347C>T | CA372621240 | SLC39A4 | c.1064G>A (p.Gly355Glu) c.989G>A (p.Gly330Glu) c.782G>A (p.Gly261Glu) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414348C>A | CA372621241 | SLC39A4 | c.1063G>T (p.Gly355Trp) c.988G>T (p.Gly330Trp) c.781G>T (p.Gly261Trp) | |
8 | g.144414348C= | CA1826307109 | SLC39A4 | c.1063G= (p.Gly355=) c.988G= (p.Gly330=) c.781G= (p.Gly261=) | |
8 | g.144414348C>G | CA372621243 | SLC39A4 | c.1063G>C (p.Gly355Arg) c.988G>C (p.Gly330Arg) c.781G>C (p.Gly261Arg) | |
8 | g.144414348C>T | CA372621242 | SLC39A4 | c.1063G>A (p.Gly355Arg) c.988G>A (p.Gly330Arg) c.781G>A (p.Gly261Arg) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414349C>A | CA372621244 | SLC39A4 | c.1062G>T (p.Arg354Ser) c.987G>T (p.Arg329Ser) c.780G>T (p.Arg260Ser) | gnomAD v4 |
8 | g.144414349C>G | CA372621245 | SLC39A4 | c.1062G>C (p.Arg354Ser) c.987G>C (p.Arg329Ser) c.780G>C (p.Arg260Ser) | gnomAD v4 |
8 | g.144414349C>T | CA463449666 | SLC39A4 | c.1062G>A (p.Arg354=) c.987G>A (p.Arg329=) c.780G>A (p.Arg260=) | ClinVar |
8 | g.144414354_144414355insCTGGCTGCAGGGGGGTCGCCCACTACATCCTGCA | CA2843154466 | SLC39A4 | c.1062_1063insATGTAGTGGGCGACCCCCCTGCAGCCAGTGCAGG (p.Gly355MetfsTer2) c.987_988insATGTAGTGGGCGACCCCCCTGCAGCCAGTGCAGG (p.Gly330MetfsTer2) c.780_781insATGTAGTGGGCGACCCCCCTGCAGCCAGTGCAGG (p.Gly261MetfsTer2) | |
8 | g.144414350C>A | CA372621246 | SLC39A4 | c.1061G>T (p.Arg354Met) c.986G>T (p.Arg329Met) c.779G>T (p.Arg260Met) | gnomAD v4 |
8 | g.144414350C= | CA1826307110 | SLC39A4 | c.1061G= (p.Arg354=) c.986G= (p.Arg329=) c.779G= (p.Arg260=) | |
8 | g.144414350C>G | CA372621247 | SLC39A4 | c.1061G>C (p.Arg354Thr) c.986G>C (p.Arg329Thr) c.779G>C (p.Arg260Thr) | gnomAD v4 |
8 | g.144414350C>T | CA4941414 | SLC39A4 | c.1061G>A (p.Arg354Lys) c.986G>A (p.Arg329Lys) c.779G>A (p.Arg260Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.144414351T>A | CA372621248 | SLC39A4 | c.1060A>T (p.Arg354Trp) c.985A>T (p.Arg329Trp) c.778A>T (p.Arg260Trp) | |
8 | g.144414351T>C | CA372621249 | SLC39A4 | c.1060A>G (p.Arg354Gly) c.985A>G (p.Arg329Gly) c.778A>G (p.Arg260Gly) | |
8 | g.144414351T>G | CA463449668 | SLC39A4 | c.1060A>C (p.Arg354=) c.985A>C (p.Arg329=) c.778A>C (p.Arg260=) | gnomAD v4 |
8 | g.144414352G>A | CA463449669 | SLC39A4 | c.1059C>T (p.Cys353=) c.984C>T (p.Cys328=) c.777C>T (p.Cys259=) | gnomAD v4 |
8 | g.144414352G>C | CA372621250 | SLC39A4 | c.1059C>G (p.Cys353Trp) c.984C>G (p.Cys328Trp) c.777C>G (p.Cys259Trp) | ClinVar dbSNP |
8 | g.144414352G= | CA1826307111 | SLC39A4 | c.1059C= (p.Cys353=) c.984C= (p.Cys328=) c.777C= (p.Cys259=) | |
8 | g.144414352G>T | CA372621251 | SLC39A4 | c.1059C>A (p.Cys353Ter) c.984C>A (p.Cys328Ter) c.777C>A (p.Cys259Ter) | gnomAD v4 |
8 | g.144414353C>A | CA372621252 | SLC39A4 | c.1058G>T (p.Cys353Phe) c.983G>T (p.Cys328Phe) c.776G>T (p.Cys259Phe) | gnomAD v4 |
8 | g.144414353C>G | CA372621253 | SLC39A4 | c.1058G>C (p.Cys353Ser) c.983G>C (p.Cys328Ser) c.776G>C (p.Cys259Ser) | |
8 | g.144414353C>T | CA372621254 | SLC39A4 | c.1058G>A (p.Cys353Tyr) c.983G>A (p.Cys328Tyr) c.776G>A (p.Cys259Tyr) | |
8 | g.144414354A= | CA1826307112 | SLC39A4 | c.1057T= (p.Cys353=) c.982T= (p.Cys328=) c.775T= (p.Cys259=) | |
8 | g.144414354A>C | CA372621257 | SLC39A4 | c.1057T>G (p.Cys353Gly) c.982T>G (p.Cys328Gly) c.775T>G (p.Cys259Gly) | |
8 | g.144414354A>G | CA372621255 | SLC39A4 | c.1057T>C (p.Cys353Arg) c.982T>C (p.Cys328Arg) c.775T>C (p.Cys259Arg) | dbSNP gnomAD v4 |
8 | g.144414354A>T | CA372621256 | SLC39A4 | c.1057T>A (p.Cys353Ser) c.982T>A (p.Cys328Ser) c.775T>A (p.Cys259Ser) | |
8 | g.144414356_144414378del | CA2689098813 | SLC39A4 | c.1035_1057del (p.Leu346GlnfsTer?) c.960_982del (p.Leu321GlnfsTer?) c.753_775del (p.Leu252GlnfsTer?) | gnomAD v4 |
8 | g.144414355G>A | CA4941415 | SLC39A4 | c.1056C>T (p.Gly352=) c.981C>T (p.Gly327=) c.774C>T (p.Gly258=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414355G>C | CA463449670 | SLC39A4 | c.1056C>G (p.Gly352=) c.981C>G (p.Gly327=) c.774C>G (p.Gly258=) | |
8 | g.144414355G= | CA1826307113 | SLC39A4 | c.1056C= (p.Gly352=) c.981C= (p.Gly327=) c.774C= (p.Gly258=) | |
8 | g.144414355G>T | CA463449672 | SLC39A4 | c.1056C>A (p.Gly352=) c.981C>A (p.Gly327=) c.774C>A (p.Gly258=) | gnomAD v4 |
8 | g.144414356C>A | CA372621258 | SLC39A4 | c.1055G>T (p.Gly352Val) c.980G>T (p.Gly327Val) c.773G>T (p.Gly258Val) | |
8 | g.144414356C>G | CA372621259 | SLC39A4 | c.1055G>C (p.Gly352Ala) c.980G>C (p.Gly327Ala) c.773G>C (p.Gly258Ala) | |
8 | g.144414356C>T | CA372621260 | SLC39A4 | c.1055G>A (p.Gly352Asp) c.980G>A (p.Gly327Asp) c.773G>A (p.Gly258Asp) | gnomAD v4 |
8 | g.144414357dup | CA2843154467 | SLC39A4 | c.1055dup (p.Cys353LeufsTer?) c.980dup (p.Cys328LeufsTer?) c.773dup (p.Cys259LeufsTer?) | |
8 | g.144414357C>A | CA372621261 | SLC39A4 | c.1054G>T (p.Gly352Cys) c.979G>T (p.Gly327Cys) c.772G>T (p.Gly258Cys) | gnomAD v4 |
8 | g.144414357C= | CA1826307114 | SLC39A4 | c.1054G= (p.Gly352=) c.979G= (p.Gly327=) c.772G= (p.Gly258=) | |
8 | g.144414357C>G | CA372621262 | SLC39A4 | c.1054G>C (p.Gly352Arg) c.979G>C (p.Gly327Arg) c.772G>C (p.Gly258Arg) | |
8 | g.144414357C>T | CA372621263 | SLC39A4 | c.1054G>A (p.Gly352Ser) c.979G>A (p.Gly327Ser) c.772G>A (p.Gly258Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414358A= | CA1826307115 | SLC39A4 | c.1053T= (p.Thr351=) c.978T= (p.Thr326=) c.771T= (p.Thr257=) | |
8 | g.144414358A>C | CA463449673 | SLC39A4 | c.1053T>G (p.Thr351=) c.978T>G (p.Thr326=) c.771T>G (p.Thr257=) | |
8 | g.144414358A>G | CA463449674 | SLC39A4 | c.1053T>C (p.Thr351=) c.978T>C (p.Thr326=) c.771T>C (p.Thr257=) | dbSNP |
8 | g.144414358A>T | CA463449675 | SLC39A4 | c.1053T>A (p.Thr351=) c.978T>A (p.Thr326=) c.771T>A (p.Thr257=) | |
8 | g.144414359G>A | CA372621264 | SLC39A4 | c.1052C>T (p.Thr351Ile) c.977C>T (p.Thr326Ile) c.770C>T (p.Thr257Ile) | gnomAD v4 |
8 | g.144414359G>C | CA372621265 | SLC39A4 | c.1052C>G (p.Thr351Ser) c.977C>G (p.Thr326Ser) c.770C>G (p.Thr257Ser) | gnomAD v4 |
8 | g.144414359G>T | CA372621266 | SLC39A4 | c.1052C>A (p.Thr351Asn) c.977C>A (p.Thr326Asn) c.770C>A (p.Thr257Asn) | |
8 | g.144414360T>A | CA372621268 | SLC39A4 | c.1051A>T (p.Thr351Ser) c.976A>T (p.Thr326Ser) c.769A>T (p.Thr257Ser) | |
8 | g.144414360T>C | CA4941416 | SLC39A4 | c.1051A>G (p.Thr351Ala) c.976A>G (p.Thr326Ala) c.769A>G (p.Thr257Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414360T>G | CA372621267 | SLC39A4 | c.1051A>C (p.Thr351Pro) c.976A>C (p.Thr326Pro) c.769A>C (p.Thr257Pro) | |
8 | g.144414360T= | CA1826307116 | SLC39A4 | c.1051A= (p.Thr351=) c.976A= (p.Thr326=) c.769A= (p.Thr257=) | |
8 | g.144414361G>A | CA463449678 | SLC39A4 | c.1050C>T (p.Cys350=) c.975C>T (p.Cys325=) c.768C>T (p.Cys256=) | gnomAD v4 |
8 | g.144414361G>C | CA372621269 | SLC39A4 | c.1050C>G (p.Cys350Trp) c.975C>G (p.Cys325Trp) c.768C>G (p.Cys256Trp) | |
8 | g.144414361G>T | CA372621270 | SLC39A4 | c.1050C>A (p.Cys350Ter) c.975C>A (p.Cys325Ter) c.768C>A (p.Cys256Ter) | gnomAD v4 |
8 | g.144414362C>A | CA372621271 | SLC39A4 | c.1049G>T (p.Cys350Phe) c.974G>T (p.Cys325Phe) c.767G>T (p.Cys256Phe) | dbSNP |
8 | g.144414362C= | CA1826307117 | SLC39A4 | c.1049G= (p.Cys350=) c.974G= (p.Cys325=) c.767G= (p.Cys256=) | |
8 | g.144414362C>G | CA372621272 | SLC39A4 | c.1049G>C (p.Cys350Ser) c.974G>C (p.Cys325Ser) c.767G>C (p.Cys256Ser) | dbSNP gnomAD v4 |
8 | g.144414362C>T | CA372621273 | SLC39A4 | c.1049G>A (p.Cys350Tyr) c.974G>A (p.Cys325Tyr) c.767G>A (p.Cys256Tyr) | dbSNP gnomAD v4 |
8 | g.144414363A>C | CA372621274 | SLC39A4 | c.1048T>G (p.Cys350Gly) c.973T>G (p.Cys325Gly) c.766T>G (p.Cys256Gly) | |
8 | g.144414363A>G | CA372621275 | SLC39A4 | c.1048T>C (p.Cys350Arg) c.973T>C (p.Cys325Arg) c.766T>C (p.Cys256Arg) | gnomAD v4 |
8 | g.144414363A>T | CA372621276 | SLC39A4 | c.1048T>A (p.Cys350Ser) c.973T>A (p.Cys325Ser) c.766T>A (p.Cys256Ser) | |
8 | g.144414364G>A | CA463449681 | SLC39A4 | c.1047C>T (p.Thr349=) c.972C>T (p.Thr324=) c.765C>T (p.Thr255=) | gnomAD v4 |
8 | g.144414364G>C | CA463449684 | SLC39A4 | c.1047C>G (p.Thr349=) c.972C>G (p.Thr324=) c.765C>G (p.Thr255=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.144414364G= | CA1826307118 | SLC39A4 | c.1047C= (p.Thr349=) c.972C= (p.Thr324=) c.765C= (p.Thr255=) | |
8 | g.144414364G>T | CA463449682 | SLC39A4 | c.1047C>A (p.Thr349=) c.972C>A (p.Thr324=) c.765C>A (p.Thr255=) | gnomAD v4 |
8 | g.144414364_144414370dup | CA2689098887 | SLC39A4 | c.1041_1047dup (p.Cys350AlafsTer?) c.966_972dup (p.Cys325AlafsTer?) c.759_765dup (p.Cys256AlafsTer?) | gnomAD v4 |
8 | g.144414365G>A | CA372621277 | SLC39A4 | c.1046C>T (p.Thr349Ile) c.971C>T (p.Thr324Ile) c.764C>T (p.Thr255Ile) | gnomAD v4 |
8 | g.144414365G>C | CA372621278 | SLC39A4 | c.1046C>G (p.Thr349Ser) c.971C>G (p.Thr324Ser) c.764C>G (p.Thr255Ser) | |
8 | g.144414365G= | CA1826307119 | SLC39A4 | c.1046C= (p.Thr349=) c.971C= (p.Thr324=) c.764C= (p.Thr255=) | |
8 | g.144414365G>T | CA372621279 | SLC39A4 | c.1046C>A (p.Thr349Asn) c.971C>A (p.Thr324Asn) c.764C>A (p.Thr255Asn) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414366T>A | CA372621280 | SLC39A4 | c.1045A>T (p.Thr349Ser) c.970A>T (p.Thr324Ser) c.763A>T (p.Thr255Ser) | |
8 | g.144414366T>C | CA372621281 | SLC39A4 | c.1045A>G (p.Thr349Ala) c.970A>G (p.Thr324Ala) c.763A>G (p.Thr255Ala) | gnomAD v4 |
8 | g.144414366T>G | CA372621282 | SLC39A4 | c.1045A>C (p.Thr349Pro) c.970A>C (p.Thr324Pro) c.763A>C (p.Thr255Pro) | dbSNP |
8 | g.144414366T= | CA1826307120 | SLC39A4 | c.1045A= (p.Thr349=) c.970A= (p.Thr324=) c.763A= (p.Thr255=) | |
8 | g.144414367C>A | CA463449686 | SLC39A4 | c.1044G>T (p.Leu348=) c.969G>T (p.Leu323=) c.762G>T (p.Leu254=) | |
8 | g.144414367C= | CA1826307121 | SLC39A4 | c.1044G= (p.Leu348=) c.969G= (p.Leu323=) c.762G= (p.Leu254=) | |
8 | g.144414367C>G | CA463449687 | SLC39A4 | c.1044G>C (p.Leu348=) c.969G>C (p.Leu323=) c.762G>C (p.Leu254=) | |
8 | g.144414367C>T | CA4941417 | SLC39A4 | c.1044G>A (p.Leu348=) c.969G>A (p.Leu323=) c.762G>A (p.Leu254=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.144414368A>C | CA372621283 | SLC39A4 | c.1043T>G (p.Leu348Arg) c.968T>G (p.Leu323Arg) c.761T>G (p.Leu254Arg) | |
8 | g.144414368A>G | CA372621284 | SLC39A4 | c.1043T>C (p.Leu348Pro) c.968T>C (p.Leu323Pro) c.761T>C (p.Leu254Pro) | |
8 | g.144414368A>T | CA372621285 | SLC39A4 | c.1043T>A (p.Leu348Gln) c.968T>A (p.Leu323Gln) c.761T>A (p.Leu254Gln) | |
8 | g.144414369G>A | CA463449689 | SLC39A4 | c.1042C>T (p.Leu348=) c.967C>T (p.Leu323=) c.760C>T (p.Leu254=) | gnomAD v4 |
8 | g.144414369G>C | CA372621286 | SLC39A4 | c.1042C>G (p.Leu348Val) c.967C>G (p.Leu323Val) c.760C>G (p.Leu254Val) | |
8 | g.144414369G>T | CA372621287 | SLC39A4 | c.1042C>A (p.Leu348Met) c.967C>A (p.Leu323Met) c.760C>A (p.Leu254Met) | |
8 | g.144414370C>A | CA463449690 | SLC39A4 | c.1041G>T (p.Leu347=) c.966G>T (p.Leu322=) c.759G>T (p.Leu253=) | gnomAD v4 |
8 | g.144414370C>G | CA463449691 | SLC39A4 | c.1041G>C (p.Leu347=) c.966G>C (p.Leu322=) c.759G>C (p.Leu253=) | |
8 | g.144414370C>T | CA463449692 | SLC39A4 | c.1041G>A (p.Leu347=) c.966G>A (p.Leu322=) c.759G>A (p.Leu253=) | |
8 | g.144414371A>C | CA372621288 | SLC39A4 | c.1040T>G (p.Leu347Arg) c.965T>G (p.Leu322Arg) c.758T>G (p.Leu253Arg) | |
8 | g.144414371A>G | CA372621289 | SLC39A4 | c.1040T>C (p.Leu347Pro) c.965T>C (p.Leu322Pro) c.758T>C (p.Leu253Pro) | |
8 | g.144414371A>T | CA372621290 | SLC39A4 | c.1040T>A (p.Leu347Gln) c.965T>A (p.Leu322Gln) c.758T>A (p.Leu253Gln) | |
8 | g.144414372G>A | CA463449693 | SLC39A4 | c.1039C>T (p.Leu347=) c.964C>T (p.Leu322=) c.757C>T (p.Leu253=) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414372G>C | CA372621291 | SLC39A4 | c.1039C>G (p.Leu347Val) c.964C>G (p.Leu322Val) c.757C>G (p.Leu253Val) | |
8 | g.144414372G= | CA1826307122 | SLC39A4 | c.1039C= (p.Leu347=) c.964C= (p.Leu322=) c.757C= (p.Leu253=) | |
8 | g.144414372G>T | CA372621292 | SLC39A4 | c.1039C>A (p.Leu347Met) c.964C>A (p.Leu322Met) c.757C>A (p.Leu253Met) | gnomAD v4 |
8 | g.144414373C>A | CA463449695 | SLC39A4 | c.1038G>T (p.Leu346=) c.963G>T (p.Leu321=) c.756G>T (p.Leu252=) | gnomAD v4 |
8 | g.144414373C>G | CA463449696 | SLC39A4 | c.1038G>C (p.Leu346=) c.963G>C (p.Leu321=) c.756G>C (p.Leu252=) | |
8 | g.144414373C>T | CA463449697 | SLC39A4 | c.1038G>A (p.Leu346=) c.963G>A (p.Leu321=) c.756G>A (p.Leu252=) | ClinVar dbSNP |
8 | g.144414374A>C | CA372621293 | SLC39A4 | c.1037T>G (p.Leu346Arg) c.962T>G (p.Leu321Arg) c.755T>G (p.Leu252Arg) | |
8 | g.144414374A>G | CA372621294 | SLC39A4 | c.1037T>C (p.Leu346Pro) c.962T>C (p.Leu321Pro) c.755T>C (p.Leu252Pro) | |
8 | g.144414374A>T | CA372621295 | SLC39A4 | c.1037T>A (p.Leu346Gln) c.962T>A (p.Leu321Gln) c.755T>A (p.Leu252Gln) | |
8 | g.144414375G>A | CA463449698 | SLC39A4 | c.1036C>T (p.Leu346=) c.961C>T (p.Leu321=) c.754C>T (p.Leu252=) | gnomAD v4 |
8 | g.144414375G>C | CA372621296 | SLC39A4 | c.1036C>G (p.Leu346Val) c.961C>G (p.Leu321Val) c.754C>G (p.Leu252Val) | |
8 | g.144414375G= | CA1826307123 | SLC39A4 | c.1036C= (p.Leu346=) c.961C= (p.Leu321=) c.754C= (p.Leu252=) | |
8 | g.144414375G>T | CA372621297 | SLC39A4 | c.1036C>A (p.Leu346Met) c.961C>A (p.Leu321Met) c.754C>A (p.Leu252Met) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414376G>A | CA463449699 | SLC39A4 | c.1035C>T (p.Leu345=) c.960C>T (p.Leu320=) c.753C>T (p.Leu251=) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414376G>C | CA463449700 | SLC39A4 | c.1035C>G (p.Leu345=) c.960C>G (p.Leu320=) c.753C>G (p.Leu251=) | ClinVar dbSNP gnomAD v4 |
8 | g.144414376G= | CA1826307124 | SLC39A4 | c.1035C= (p.Leu345=) c.960C= (p.Leu320=) c.753C= (p.Leu251=) | |
8 | g.144414376G>T | CA4941418 | SLC39A4 | c.1035C>A (p.Leu345=) c.960C>A (p.Leu320=) c.753C>A (p.Leu251=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414377A>C | CA372621298 | SLC39A4 | c.1034T>G (p.Leu345Arg) c.959T>G (p.Leu320Arg) c.752T>G (p.Leu251Arg) | |
8 | g.144414377A>G | CA372621299 | SLC39A4 | c.1034T>C (p.Leu345Pro) c.959T>C (p.Leu320Pro) c.752T>C (p.Leu251Pro) | gnomAD v4 |
8 | g.144414377A>T | CA372621300 | SLC39A4 | c.1034T>A (p.Leu345His) c.959T>A (p.Leu320His) c.752T>A (p.Leu251His) | |
8 | g.144414378G>A | CA372621301 | SLC39A4 | c.1033C>T (p.Leu345Phe) c.958C>T (p.Leu320Phe) c.751C>T (p.Leu251Phe) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414378G>C | CA372621302 | SLC39A4 | c.1033C>G (p.Leu345Val) c.958C>G (p.Leu320Val) c.751C>G (p.Leu251Val) | |
8 | g.144414378G= | CA1826307125 | SLC39A4 | c.1033C= (p.Leu345=) c.958C= (p.Leu320=) c.751C= (p.Leu251=) | |
8 | g.144414378G>T | CA372621303 | SLC39A4 | c.1033C>A (p.Leu345Ile) c.958C>A (p.Leu320Ile) c.751C>A (p.Leu251Ile) | gnomAD v4 |
8 | g.144414379dup | CA2689098921 | SLC39A4 | c.1033dup (p.Leu345ProfsTer?) c.958dup (p.Leu320ProfsTer?) c.751dup (p.Leu251ProfsTer?) | gnomAD v4 |
8 | g.144414379G>A | CA463449701 | SLC39A4 | c.1032C>T (p.Gly344=) c.957C>T (p.Gly319=) c.750C>T (p.Gly250=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414379G>C | CA463449702 | SLC39A4 | c.1032C>G (p.Gly344=) c.957C>G (p.Gly319=) c.750C>G (p.Gly250=) | |
8 | g.144414379G= | CA1826307126 | SLC39A4 | c.1032C= (p.Gly344=) c.957C= (p.Gly319=) c.750C= (p.Gly250=) | |
8 | g.144414379G>T | CA463449703 | SLC39A4 | c.1032C>A (p.Gly344=) c.957C>A (p.Gly319=) c.750C>A (p.Gly250=) | ClinVar dbSNP gnomAD v4 |
8 | g.144414380C>A | CA372621305 | SLC39A4 | c.1031G>T (p.Gly344Val) c.956G>T (p.Gly319Val) c.749G>T (p.Gly250Val) | |
8 | g.144414380C= | CA1826307127 | SLC39A4 | c.1031G= (p.Gly344=) c.956G= (p.Gly319=) c.749G= (p.Gly250=) | |
8 | g.144414380C>G | CA372621304 | SLC39A4 | c.1031G>C (p.Gly344Ala) c.956G>C (p.Gly319Ala) c.749G>C (p.Gly250Ala) | |
8 | g.144414380C>T | CA4941419 | SLC39A4 | c.1031G>A (p.Gly344Asp) c.956G>A (p.Gly319Asp) c.749G>A (p.Gly250Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.144414381C>A | CA372621306 | SLC39A4 | c.1030G>T (p.Gly344Cys) c.955G>T (p.Gly319Cys) c.748G>T (p.Gly250Cys) | |
8 | g.144414381C= | CA1826307128 | SLC39A4 | c.1030G= (p.Gly344=) c.955G= (p.Gly319=) c.748G= (p.Gly250=) | |
8 | g.144414381C>G | CA372621307 | SLC39A4 | c.1030G>C (p.Gly344Arg) c.955G>C (p.Gly319Arg) c.748G>C (p.Gly250Arg) | |
8 | g.144414381C>T | CA372621308 | SLC39A4 | c.1030G>A (p.Gly344Ser) c.955G>A (p.Gly319Ser) c.748G>A (p.Gly250Ser) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414382A>C | CA372621309 | SLC39A4 | c.1029T>G (p.Phe343Leu) c.954T>G (p.Phe318Leu) c.747T>G (p.Phe249Leu) | |
8 | g.144414382A>G | CA463449705 | SLC39A4 | c.1029T>C (p.Phe343=) c.954T>C (p.Phe318=) c.747T>C (p.Phe249=) | |
8 | g.144414382A>T | CA372621310 | SLC39A4 | c.1029T>A (p.Phe343Leu) c.954T>A (p.Phe318Leu) c.747T>A (p.Phe249Leu) | |
8 | g.144414383A= | CA1826307129 | SLC39A4 | c.1028T= (p.Phe343=) c.953T= (p.Phe318=) c.746T= (p.Phe249=) | |
8 | g.144414383A>C | CA372621311 | SLC39A4 | c.1028T>G (p.Phe343Cys) c.953T>G (p.Phe318Cys) c.746T>G (p.Phe249Cys) | |
8 | g.144414383A>G | CA372621313 | SLC39A4 | c.1028T>C (p.Phe343Ser) c.953T>C (p.Phe318Ser) c.746T>C (p.Phe249Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414383A>T | CA372621312 | SLC39A4 | c.1028T>A (p.Phe343Tyr) c.953T>A (p.Phe318Tyr) c.746T>A (p.Phe249Tyr) | |
8 | g.144414384A>C | CA372621314 | SLC39A4 | c.1027T>G (p.Phe343Val) c.952T>G (p.Phe318Val) c.745T>G (p.Phe249Val) | |
8 | g.144414384A>G | CA372621315 | SLC39A4 | c.1027T>C (p.Phe343Leu) c.952T>C (p.Phe318Leu) c.745T>C (p.Phe249Leu) | |
8 | g.144414384A>T | CA372621316 | SLC39A4 | c.1027T>A (p.Phe343Ile) c.952T>A (p.Phe318Ile) c.745T>A (p.Phe249Ile) | |
8 | g.144414385G>A | CA463449707 | SLC39A4 | c.1026C>T (p.Val342=) c.951C>T (p.Val317=) c.744C>T (p.Val248=) | gnomAD v4 |
8 | g.144414385G>C | CA463449708 | SLC39A4 | c.1026C>G (p.Val342=) c.951C>G (p.Val317=) c.744C>G (p.Val248=) | gnomAD v4 |
8 | g.144414385G>T | CA463449709 | SLC39A4 | c.1026C>A (p.Val342=) c.951C>A (p.Val317=) c.744C>A (p.Val248=) | gnomAD v4 |
8 | g.144414386A= | CA1826307130 | SLC39A4 | c.1025T= (p.Val342=) c.950T= (p.Val317=) c.743T= (p.Val248=) | |
8 | g.144414386A>C | CA372621317 | SLC39A4 | c.1025T>G (p.Val342Gly) c.950T>G (p.Val317Gly) c.743T>G (p.Val248Gly) | |
8 | g.144414386A>G | CA372621318 | SLC39A4 | c.1025T>C (p.Val342Ala) c.950T>C (p.Val317Ala) c.743T>C (p.Val248Ala) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.144414386A>T | CA372621319 | SLC39A4 | c.1025T>A (p.Val342Asp) c.950T>A (p.Val317Asp) c.743T>A (p.Val248Asp) | |
8 | g.144414387C>A | CA372621320 | SLC39A4 | c.1024G>T (p.Val342Phe) c.949G>T (p.Val317Phe) c.742G>T (p.Val248Phe) | gnomAD v4 |
8 | g.144414387C>G | CA372621321 | SLC39A4 | c.1024G>C (p.Val342Leu) c.949G>C (p.Val317Leu) c.742G>C (p.Val248Leu) | |
8 | g.144414387C>T | CA372621322 | SLC39A4 | c.1024G>A (p.Val342Ile) c.949G>A (p.Val317Ile) c.742G>A (p.Val248Ile) | |
8 | g.144414388C>A | CA463449710 | SLC39A4 | c.1023G>T (p.Ala341=) c.948G>T (p.Ala316=) c.741G>T (p.Ala247=) | |
8 | g.144414388C= | CA1826307131 | SLC39A4 | c.1023G= (p.Ala341=) c.948G= (p.Ala316=) c.741G= (p.Ala247=) | |
8 | g.144414388C>G | CA4941421 | SLC39A4 | c.1023G>C (p.Ala341=) c.948G>C (p.Ala316=) c.741G>C (p.Ala247=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414388C>T | CA4941420 | SLC39A4 | c.1023G>A (p.Ala341=) c.948G>A (p.Ala316=) c.741G>A (p.Ala247=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414389G>A | CA4941422 | SLC39A4 | c.1022C>T (p.Ala341Val) c.947C>T (p.Ala316Val) c.740C>T (p.Ala247Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414389G>C | CA372621324 | SLC39A4 | c.1022C>G (p.Ala341Gly) c.947C>G (p.Ala316Gly) c.740C>G (p.Ala247Gly) | |
8 | g.144414389G= | CA1826307132 | SLC39A4 | c.1022C= (p.Ala341=) c.947C= (p.Ala316=) c.740C= (p.Ala247=) | |
8 | g.144414389G>T | CA372621323 | SLC39A4 | c.1022C>A (p.Ala341Glu) c.947C>A (p.Ala316Glu) c.740C>A (p.Ala247Glu) | gnomAD v4 |
8 | g.144414390C>A | CA372621325 | SLC39A4 | c.1021G>T (p.Ala341Ser) c.946G>T (p.Ala316Ser) c.739G>T (p.Ala247Ser) | ClinVar gnomAD v4 |
8 | g.144414390C= | CA1826307133 | SLC39A4 | c.1021G= (p.Ala341=) c.946G= (p.Ala316=) c.739G= (p.Ala247=) | |
8 | g.144414390C>G | CA372621326 | SLC39A4 | c.1021G>C (p.Ala341Pro) c.946G>C (p.Ala316Pro) c.739G>C (p.Ala247Pro) | |
8 | g.144414390C>T | CA4941423 | SLC39A4 | c.1021G>A (p.Ala341Thr) c.946G>A (p.Ala316Thr) c.739G>A (p.Ala247Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414391G>A | CA4941424 | SLC39A4 | c.1020C>T (p.Cys340=) c.945C>T (p.Cys315=) c.738C>T (p.Cys246=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414391G>C | CA372621327 | SLC39A4 | c.1020C>G (p.Cys340Trp) c.945C>G (p.Cys315Trp) c.738C>G (p.Cys246Trp) | gnomAD v4 |
8 | g.144414391G= | CA1826307135 | SLC39A4 | c.1020C= (p.Cys340=) c.945C= (p.Cys315=) c.738C= (p.Cys246=) | |
8 | g.144414391G>T | CA372621328 | SLC39A4 | c.1020C>A (p.Cys340Ter) c.945C>A (p.Cys315Ter) c.738C>A (p.Cys246Ter) | dbSNP gnomAD v4 |
8 | g.144414392_144414400dup | CA1826307134 | SLC39A4 | c.1012_1020dup (p.Cys340_Ala341insCysLeuCys) c.937_945dup (p.Cys315_Ala316insCysLeuCys) c.730_738dup (p.Cys246_Ala247insCysLeuCys) | dbSNP |
8 | g.144414393_144414409dup | CA915947392 | SLC39A4 | c.1004_1020dup (p.Ala341CysfsTer14) c.929_945dup (p.Ala316CysfsTer14) c.722_738dup (p.Ala247CysfsTer14) | ClinVar dbSNP |
8 | g.144414392C>A | CA372621329 | SLC39A4 | c.1019G>T (p.Cys340Phe) c.944G>T (p.Cys315Phe) c.737G>T (p.Cys246Phe) | gnomAD v4 |
8 | g.144414392C>G | CA372621330 | SLC39A4 | c.1019G>C (p.Cys340Ser) c.944G>C (p.Cys315Ser) c.737G>C (p.Cys246Ser) | |
8 | g.144414392C>T | CA372621331 | SLC39A4 | c.1019G>A (p.Cys340Tyr) c.944G>A (p.Cys315Tyr) c.737G>A (p.Cys246Tyr) | gnomAD v4 |
8 | g.144414393A>C | CA372621332 | SLC39A4 | c.1018T>G (p.Cys340Gly) c.943T>G (p.Cys315Gly) c.736T>G (p.Cys246Gly) | |
8 | g.144414393A>G | CA372621333 | SLC39A4 | c.1018T>C (p.Cys340Arg) c.943T>C (p.Cys315Arg) c.736T>C (p.Cys246Arg) | |
8 | g.144414393A>T | CA372621334 | SLC39A4 | c.1018T>A (p.Cys340Ser) c.943T>A (p.Cys315Ser) c.736T>A (p.Cys246Ser) | |
8 | g.144414394G>A | CA463449714 | SLC39A4 | c.1017C>T (p.Leu339=) c.942C>T (p.Leu314=) c.735C>T (p.Leu245=) | ClinVar dbSNP gnomAD v4 |
8 | g.144414394G>C | CA463449715 | SLC39A4 | c.1017C>G (p.Leu339=) c.942C>G (p.Leu314=) c.735C>G (p.Leu245=) | |
8 | g.144414394G>T | CA463449716 | SLC39A4 | c.1017C>A (p.Leu339=) c.942C>A (p.Leu314=) c.735C>A (p.Leu245=) | |
8 | g.144414395A= | CA1826307136 | SLC39A4 | c.1016T= (p.Leu339=) c.941T= (p.Leu314=) c.734T= (p.Leu245=) | |
8 | g.144414395A>C | CA372621336 | SLC39A4 | c.1016T>G (p.Leu339Arg) c.941T>G (p.Leu314Arg) c.734T>G (p.Leu245Arg) | |
8 | g.144414395A>G | CA4941425 | SLC39A4 | c.1016T>C (p.Leu339Pro) c.941T>C (p.Leu314Pro) c.734T>C (p.Leu245Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.144414395A>T | CA372621335 | SLC39A4 | c.1016T>A (p.Leu339His) c.941T>A (p.Leu314His) c.734T>A (p.Leu245His) | |
8 | g.144414395_144414398delinsAGGC | CA1826307137 | SLC39A4 | c.1013_1016delinsGCCT (p.Cys338=) c.938_941delinsGCCT (p.Cys313=) c.731_734delinsGCCT (p.Cys244=) | |
8 | g.144414396G>A | CA372621337 | SLC39A4 | c.1015C>T (p.Leu339Phe) c.940C>T (p.Leu314Phe) c.733C>T (p.Leu245Phe) | dbSNP COSMIC COSMIC |
8 | g.144414396G>C | CA372621338 | SLC39A4 | c.1015C>G (p.Leu339Val) c.940C>G (p.Leu314Val) c.733C>G (p.Leu245Val) | |
8 | g.144414396G= | CA1826307138 | SLC39A4 | c.1015C= (p.Leu339=) c.940C= (p.Leu314=) c.733C= (p.Leu245=) | |
8 | g.144414396G>T | CA372621339 | SLC39A4 | c.1015C>A (p.Leu339Ile) c.940C>A (p.Leu314Ile) c.733C>A (p.Leu245Ile) | gnomAD v4 |
8 | g.144414396_144414398del | CA586164229 | SLC39A4 | c.1013_1015del (p.Cys338_Leu339delinsPhe) c.938_940del (p.Cys313_Leu314delinsPhe) c.731_733del (p.Cys244_Leu245delinsPhe) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414397G>A | CA463449718 | SLC39A4 | c.1014C>T (p.Cys338=) c.939C>T (p.Cys313=) c.732C>T (p.Cys244=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
8 | g.144414397G>C | CA372621340 | SLC39A4 | c.1014C>G (p.Cys338Trp) c.939C>G (p.Cys313Trp) c.732C>G (p.Cys244Trp) | |
8 | g.144414397G= | CA1826307139 | SLC39A4 | c.1014C= (p.Cys338=) c.939C= (p.Cys313=) c.732C= (p.Cys244=) | |
8 | g.144414397G>T | CA372621341 | SLC39A4 | c.1014C>A (p.Cys338Ter) c.939C>A (p.Cys313Ter) c.732C>A (p.Cys244Ter) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414398C>A | CA372621342 | SLC39A4 | c.1013G>T (p.Cys338Phe) c.938G>T (p.Cys313Phe) c.731G>T (p.Cys244Phe) | |
8 | g.144414398C>G | CA372621343 | SLC39A4 | c.1013G>C (p.Cys338Ser) c.938G>C (p.Cys313Ser) c.731G>C (p.Cys244Ser) | |
8 | g.144414398C>T | CA372621344 | SLC39A4 | c.1013G>A (p.Cys338Tyr) c.938G>A (p.Cys313Tyr) c.731G>A (p.Cys244Tyr) | gnomAD v4 |
8 | g.144414399A= | CA1826307140 | SLC39A4 | c.1012T= (p.Cys338=) c.937T= (p.Cys313=) c.730T= (p.Cys244=) | |
8 | g.144414399A>C | CA372621345 | SLC39A4 | c.1012T>G (p.Cys338Gly) c.937T>G (p.Cys313Gly) c.730T>G (p.Cys244Gly) | |
8 | g.144414399A>G | CA4941426 | SLC39A4 | c.1012T>C (p.Cys338Arg) c.937T>C (p.Cys313Arg) c.730T>C (p.Cys244Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414399A>T | CA372621346 | SLC39A4 | c.1012T>A (p.Cys338Ser) c.937T>A (p.Cys313Ser) c.730T>A (p.Cys244Ser) | |
8 | g.144414400G>A | CA463449720 | SLC39A4 | c.1011C>T (p.Ile337=) c.936C>T (p.Ile312=) c.729C>T (p.Ile243=) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414400G>C | CA372621347 | SLC39A4 | c.1011C>G (p.Ile337Met) c.936C>G (p.Ile312Met) c.729C>G (p.Ile243Met) | |
8 | g.144414400G= | CA1826307141 | SLC39A4 | c.1011C= (p.Ile337=) c.936C= (p.Ile312=) c.729C= (p.Ile243=) | |
8 | g.144414400G>T | CA463449719 | SLC39A4 | c.1011C>A (p.Ile337=) c.936C>A (p.Ile312=) c.729C>A (p.Ile243=) | gnomAD v4 |
8 | g.144414401A>C | CA372621349 | SLC39A4 | c.1010T>G (p.Ile337Ser) c.935T>G (p.Ile312Ser) c.728T>G (p.Ile243Ser) | |
8 | g.144414401A>G | CA372621350 | SLC39A4 | c.1010T>C (p.Ile337Thr) c.935T>C (p.Ile312Thr) c.728T>C (p.Ile243Thr) | |
8 | g.144414401A>T | CA372621348 | SLC39A4 | c.1010T>A (p.Ile337Asn) c.935T>A (p.Ile312Asn) c.728T>A (p.Ile243Asn) | |
8 | g.144414402T>A | CA372621352 | SLC39A4 | c.1009A>T (p.Ile337Phe) c.934A>T (p.Ile312Phe) c.727A>T (p.Ile243Phe) | gnomAD v4 |
8 | g.144414402T>C | CA372621351 | SLC39A4 | c.1009A>G (p.Ile337Val) c.934A>G (p.Ile312Val) c.727A>G (p.Ile243Val) | |
8 | g.144414402T>G | CA372621353 | SLC39A4 | c.1009A>C (p.Ile337Leu) c.934A>C (p.Ile312Leu) c.727A>C (p.Ile243Leu) | gnomAD v4 |
8 | g.144414403G>A | CA4941427 | SLC39A4 | c.1008C>T (p.Leu336=) c.933C>T (p.Leu311=) c.726C>T (p.Leu242=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414403G>C | CA463449724 | SLC39A4 | c.1008C>G (p.Leu336=) c.933C>G (p.Leu311=) c.726C>G (p.Leu242=) | gnomAD v4 |
8 | g.144414403G= | CA1826307142 | SLC39A4 | c.1008C= (p.Leu336=) c.933C= (p.Leu311=) c.726C= (p.Leu242=) | |
8 | g.144414403G>T | CA463449725 | SLC39A4 | c.1008C>A (p.Leu336=) c.933C>A (p.Leu311=) c.726C>A (p.Leu242=) | |
8 | g.144414404A>C | CA372621354 | SLC39A4 | c.1007T>G (p.Leu336Arg) c.932T>G (p.Leu311Arg) c.725T>G (p.Leu242Arg) | |
8 | g.144414404A>G | CA372621355 | SLC39A4 | c.1007T>C (p.Leu336Pro) c.932T>C (p.Leu311Pro) c.725T>C (p.Leu242Pro) | |
8 | g.144414404A>T | CA372621356 | SLC39A4 | c.1007T>A (p.Leu336His) c.932T>A (p.Leu311His) c.725T>A (p.Leu242His) | gnomAD v4 |
8 | g.144414405G>A | CA372621357 | SLC39A4 | c.1006C>T (p.Leu336Phe) c.931C>T (p.Leu311Phe) c.724C>T (p.Leu242Phe) | |
8 | g.144414405G>C | CA372621358 | SLC39A4 | c.1006C>G (p.Leu336Val) c.931C>G (p.Leu311Val) c.724C>G (p.Leu242Val) | |
8 | g.144414405G>T | CA372621359 | SLC39A4 | c.1006C>A (p.Leu336Ile) c.931C>A (p.Leu311Ile) c.724C>A (p.Leu242Ile) | |
8 | g.144414406C>A | CA463449726 | SLC39A4 | c.1005G>T (p.Leu335=) c.930G>T (p.Leu310=) c.723G>T (p.Leu241=) | |
8 | g.144414406C= | CA1826307143 | SLC39A4 | c.1005G= (p.Leu335=) c.930G= (p.Leu310=) c.723G= (p.Leu241=) | |
8 | g.144414406C>G | CA463449727 | SLC39A4 | c.1005G>C (p.Leu335=) c.930G>C (p.Leu310=) c.723G>C (p.Leu241=) | |
8 | g.144414406C>T | CA187648312 | SLC39A4 | c.1005G>A (p.Leu335=) c.930G>A (p.Leu310=) c.723G>A (p.Leu241=) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.144414407A>C | CA372621360 | SLC39A4 | c.1004T>G (p.Leu335Arg) c.929T>G (p.Leu310Arg) c.722T>G (p.Leu241Arg) | |
8 | g.144414407A>G | CA372621361 | SLC39A4 | c.1004T>C (p.Leu335Pro) c.929T>C (p.Leu310Pro) c.722T>C (p.Leu241Pro) | |
8 | g.144414407A>T | CA372621362 | SLC39A4 | c.1004T>A (p.Leu335Gln) c.929T>A (p.Leu310Gln) c.722T>A (p.Leu241Gln) | |
8 | g.144414408G>A | CA4941428 | SLC39A4 | c.1003C>T (p.Leu335=) c.928C>T (p.Leu310=) c.721C>T (p.Leu241=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414408G>C | CA372621363 | SLC39A4 | c.1003C>G (p.Leu335Val) c.928C>G (p.Leu310Val) c.721C>G (p.Leu241Val) | |
8 | g.144414408G= | CA1826307144 | SLC39A4 | c.1003C= (p.Leu335=) c.928C= (p.Leu310=) c.721C= (p.Leu241=) | |
8 | g.144414408G>T | CA372621364 | SLC39A4 | c.1003C>A (p.Leu335Met) c.928C>A (p.Leu310Met) c.721C>A (p.Leu241Met) | gnomAD v4 |
8 | g.144414409C>A | CA463449728 | SLC39A4 | c.1002G>T (p.Thr334=) c.927G>T (p.Thr309=) c.720G>T (p.Thr240=) | gnomAD v4 COSMIC COSMIC |
8 | g.144414409C= | CA1826307145 | SLC39A4 | c.1002G= (p.Thr334=) c.927G= (p.Thr309=) c.720G= (p.Thr240=) | |
8 | g.144414409C>G | CA463449729 | SLC39A4 | c.1002G>C (p.Thr334=) c.927G>C (p.Thr309=) c.720G>C (p.Thr240=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.144414409C>T | CA4941429 | SLC39A4 | c.1002G>A (p.Thr334=) c.927G>A (p.Thr309=) c.720G>A (p.Thr240=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414410G>A | CA4941430 | SLC39A4 | c.1001C>T (p.Thr334Met) c.926C>T (p.Thr309Met) c.719C>T (p.Thr240Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.144414410G>C | CA372621365 | SLC39A4 | c.1001C>G (p.Thr334Arg) c.926C>G (p.Thr309Arg) c.719C>G (p.Thr240Arg) | |
8 | g.144414410G= | CA1826307146 | SLC39A4 | c.1001C= (p.Thr334=) c.926C= (p.Thr309=) c.719C= (p.Thr240=) | |
8 | g.144414410G>T | CA372621366 | SLC39A4 | c.1001C>A (p.Thr334Lys) c.926C>A (p.Thr309Lys) c.719C>A (p.Thr240Lys) | |
8 | g.144414411T>A | CA372621367 | SLC39A4 | c.1000A>T (p.Thr334Ser) c.925A>T (p.Thr309Ser) c.718A>T (p.Thr240Ser) | dbSNP gnomAD v2 |
8 | g.144414411T>C | CA372621368 | SLC39A4 | c.1000A>G (p.Thr334Ala) c.925A>G (p.Thr309Ala) c.718A>G (p.Thr240Ala) | |
8 | g.144414411T>G | CA372621369 | SLC39A4 | c.1000A>C (p.Thr334Pro) c.925A>C (p.Thr309Pro) c.718A>C (p.Thr240Pro) | |
8 | g.144414411T= | CA1826307147 | SLC39A4 | c.1000A= (p.Thr334=) c.925A= (p.Thr309=) c.718A= (p.Thr240=) |