ClinVar Miner

List of variants in gene DDX3X reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 146
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HGVS dbSNP gnomAD frequency
NM_001356.5(DDX3X):c.426A>C (p.Pro142=) rs779721240 0.00010
NM_001356.5(DDX3X):c.353A>G (p.Lys118Arg) rs759994098 0.00005
NM_001356.5(DDX3X):c.1819G>A (p.Gly607Ser) rs755359362 0.00003
NM_001356.5(DDX3X):c.1289T>A (p.Phe430Tyr) rs773694310 0.00002
NM_001356.5(DDX3X):c.1315+4A>G rs763454948 0.00002
NM_001356.5(DDX3X):c.1315+5C>T rs368731454 0.00002
NM_001356.5(DDX3X):c.236G>A (p.Arg79Lys) rs1064795656 0.00002
NM_001356.5(DDX3X):c.251T>G (p.Phe84Cys) rs892274119 0.00002
NM_001356.5(DDX3X):c.1026-3C>T rs1288221968 0.00001
NM_001356.5(DDX3X):c.1885G>A (p.Gly629Ser) rs1476609971 0.00001
NM_001356.5(DDX3X):c.348T>A (p.Phe116Leu) rs2063866358 0.00001
NM_001356.5(DDX3X):c.533A>G (p.His178Arg) rs997047370 0.00001
NM_001356.5(DDX3X):c.745G>A (p.Glu249Lys) rs752738546 0.00001
NC_000023.10:g.(?_41193506)_(41196738_?)dup
NC_000023.10:g.(?_41193506)_(41198356_?)dup
NM_001193416.3(DDX3X):c.1192G>C (p.Asp398His) rs2147356594
NM_001356.5(DDX3X):c.1019T>A (p.Phe340Tyr) rs2063893678
NM_001356.5(DDX3X):c.1025+146C>G
NM_001356.5(DDX3X):c.1025+26_1025+33del
NM_001356.5(DDX3X):c.1025+4T>G
NM_001356.5(DDX3X):c.1032G>C (p.Leu344Phe)
NM_001356.5(DDX3X):c.1037T>C (p.Leu346Ser)
NM_001356.5(DDX3X):c.1039_1040inv (p.Asp347Ser)
NM_001356.5(DDX3X):c.1091T>C (p.Ile364Thr)
NM_001356.5(DDX3X):c.1112C>T (p.Pro371Leu)
NM_001356.5(DDX3X):c.1171-11_1171-8del
NM_001356.5(DDX3X):c.1180C>T (p.Arg394Cys)
NM_001356.5(DDX3X):c.1181G>A (p.Arg394His) rs1555953865
NM_001356.5(DDX3X):c.1203C>T (p.Ile401=)
NM_001356.5(DDX3X):c.1268A>G (p.Glu423Gly) rs2147356732
NM_001356.5(DDX3X):c.133A>T (p.Asn45Tyr)
NM_001356.5(DDX3X):c.1399G>A (p.Ala467Thr) rs2147358490
NM_001356.5(DDX3X):c.1415A>C (p.His472Pro) rs2063923221
NM_001356.5(DDX3X):c.1424G>A (p.Arg475His) rs1602135832
NM_001356.5(DDX3X):c.1433G>A (p.Arg478Lys)
NM_001356.5(DDX3X):c.1454A>C (p.His485Pro) rs2063923789
NM_001356.5(DDX3X):c.1462C>T (p.Arg488Cys) rs796052234
NM_001356.5(DDX3X):c.1489G>C (p.Ala497Pro) rs1602135997
NM_001356.5(DDX3X):c.1497A>G (p.Ala499=)
NM_001356.5(DDX3X):c.1518C>G (p.Asp506Glu)
NM_001356.5(DDX3X):c.152-668T>C
NM_001356.5(DDX3X):c.1522T>C (p.Ser508Pro)
NM_001356.5(DDX3X):c.152G>A (p.Gly51Asp)
NM_001356.5(DDX3X):c.1535A>G (p.His512Arg)
NM_001356.5(DDX3X):c.1541T>G (p.Ile514Ser) rs796052226
NM_001356.5(DDX3X):c.1582C>T (p.Arg528Cys) rs1064795323
NM_001356.5(DDX3X):c.1615G>C (p.Gly539Arg) rs2147359364
NM_001356.5(DDX3X):c.1616-10A>G
NM_001356.5(DDX3X):c.1616-13G>A rs2147359855
NM_001356.5(DDX3X):c.1616-4_1616-3del rs751868529
NM_001356.5(DDX3X):c.1616-7_1616-6del rs1302694358
NM_001356.5(DDX3X):c.1648A>G (p.Ile550Val)
NM_001356.5(DDX3X):c.1676T>A (p.Leu559His) rs1064794993
NM_001356.5(DDX3X):c.1699G>C (p.Val567Leu) rs1555954386
NM_001356.5(DDX3X):c.171T>G (p.Ser57Arg)
NM_001356.5(DDX3X):c.172T>G (p.Ser58Ala) rs1555952639
NM_001356.5(DDX3X):c.1742A>G (p.Lys581Arg)
NM_001356.5(DDX3X):c.1745G>T (p.Gly582Val)
NM_001356.5(DDX3X):c.1759C>T (p.Arg587Cys)
NM_001356.5(DDX3X):c.1763C>T (p.Ser588Phe)
NM_001356.5(DDX3X):c.1781G>A (p.Ser594Asn)
NM_001356.5(DDX3X):c.179G>T (p.Trp60Leu)
NM_001356.5(DDX3X):c.1805A>G (p.Tyr602Cys)
NM_001356.5(DDX3X):c.1808G>A (p.Arg603Gln)
NM_001356.5(DDX3X):c.1815_1817del (p.Ser606del) rs2063940085
NM_001356.5(DDX3X):c.1852_1866del (p.Ala618_Arg622del)
NM_001356.5(DDX3X):c.1855AGC[2] (p.Ser621del) rs1308155746
NM_001356.5(DDX3X):c.1856G>A (p.Ser619Asn) rs2063940911
NM_001356.5(DDX3X):c.1864C>A (p.Arg622Ser)
NM_001356.5(DDX3X):c.1868G>T (p.Ser623Ile) rs1555954556
NM_001356.5(DDX3X):c.1873G>A (p.Gly625Arg)
NM_001356.5(DDX3X):c.1883A>C (p.His628Pro)
NM_001356.5(DDX3X):c.1906G>A (p.Gly636Arg) rs1351543785
NM_001356.5(DDX3X):c.1909+6G>A
NM_001356.5(DDX3X):c.1910-20_1910-17del rs1029725804
NM_001356.5(DDX3X):c.1912G>T (p.Gly638Cys)
NM_001356.5(DDX3X):c.1931A>G (p.Asn644Ser)
NM_001356.5(DDX3X):c.1949G>A (p.Gly650Glu)
NM_001356.5(DDX3X):c.194A>G (p.Asp65Gly) rs2063850443
NM_001356.5(DDX3X):c.1955A>G (p.Tyr652Cys)
NM_001356.5(DDX3X):c.1969G>A (p.Val657Ile)
NM_001356.5(DDX3X):c.1980G>A (p.Trp660Ter) rs2147361824
NM_001356.5(DDX3X):c.203C>A (p.Ala68Glu)
NM_001356.5(DDX3X):c.203C>T (p.Ala68Val)
NM_001356.5(DDX3X):c.224G>A (p.Arg75His)
NM_001356.5(DDX3X):c.226_228del (p.Ser76del)
NM_001356.5(DDX3X):c.227G>A (p.Ser76Asn)
NM_001356.5(DDX3X):c.232T>C (p.Ser78Pro)
NM_001356.5(DDX3X):c.23A>G (p.Asn8Ser) rs2147332802
NM_001356.5(DDX3X):c.245C>G (p.Ser82Cys)
NM_001356.5(DDX3X):c.250TTC[1] (p.Phe85del)
NM_001356.5(DDX3X):c.262C>T (p.Arg88Cys)
NM_001356.5(DDX3X):c.263G>A (p.Arg88His)
NM_001356.5(DDX3X):c.280G>A (p.Gly94Arg)
NM_001356.5(DDX3X):c.284+3A>T rs1188370836
NM_001356.5(DDX3X):c.285-3C>T
NM_001356.5(DDX3X):c.295C>T (p.Arg99Cys)
NM_001356.5(DDX3X):c.31G>A (p.Gly11Arg)
NM_001356.5(DDX3X):c.326G>A (p.Ser109Asn)
NM_001356.5(DDX3X):c.329G>A (p.Arg110His)
NM_001356.5(DDX3X):c.361C>T (p.Arg121Cys)
NM_001356.5(DDX3X):c.383G>A (p.Cys128Tyr)
NM_001356.5(DDX3X):c.38A>G (p.Asp13Gly) rs2147332843
NM_001356.5(DDX3X):c.402T>A (p.Asp134Glu) rs2147350596
NM_001356.5(DDX3X):c.416C>G (p.Pro139Arg)
NM_001356.5(DDX3X):c.428G>A (p.Ser143Asn)
NM_001356.5(DDX3X):c.431A>G (p.Glu144Gly)
NM_001356.5(DDX3X):c.443A>G (p.Gln148Arg) rs1064794404
NM_001356.5(DDX3X):c.444-10T>C rs2147350799
NM_001356.5(DDX3X):c.455C>T (p.Ser152Phe) rs2147350825
NM_001356.5(DDX3X):c.464A>G (p.Asn155Ser) rs2147350829
NM_001356.5(DDX3X):c.465C>A (p.Asn155Lys)
NM_001356.5(DDX3X):c.472A>G (p.Ile158Val) rs2147350838
NM_001356.5(DDX3X):c.509C>T (p.Ala170Val)
NM_001356.5(DDX3X):c.50C>G (p.Ala17Gly)
NM_001356.5(DDX3X):c.518A>G (p.Asn173Ser)
NM_001356.5(DDX3X):c.536T>C (p.Ile179Thr)
NM_001356.5(DDX3X):c.553G>A (p.Val185Ile)
NM_001356.5(DDX3X):c.569T>G (p.Ile190Ser) rs1555953152
NM_001356.5(DDX3X):c.581A>G (p.Asn194Ser) rs2063875302
NM_001356.5(DDX3X):c.585T>G (p.Ile195Met)
NM_001356.5(DDX3X):c.652_654del (p.Arg218del) rs2147351888
NM_001356.5(DDX3X):c.680-21_680-20delinsGA
NM_001356.5(DDX3X):c.719G>A (p.Ser240Asn) rs2147352891
NM_001356.5(DDX3X):c.757G>C (p.Ala253Pro)
NM_001356.5(DDX3X):c.765+4G>A
NM_001356.5(DDX3X):c.765+6T>A
NM_001356.5(DDX3X):c.765G>A (p.Lys255=)
NM_001356.5(DDX3X):c.766-12C>G
NM_001356.5(DDX3X):c.769A>C (p.Asn257His) rs2147353397
NM_001356.5(DDX3X):c.773G>T (p.Gly258Val)
NM_001356.5(DDX3X):c.778T>A (p.Tyr260Asn)
NM_001356.5(DDX3X):c.784C>T (p.Arg262Cys) rs1555953406
NM_001356.5(DDX3X):c.788G>A (p.Arg263His) rs867967504
NM_001356.5(DDX3X):c.800C>G (p.Pro267Arg)
NM_001356.5(DDX3X):c.802A>G (p.Ile268Val) rs2063889291
NM_001356.5(DDX3X):c.80A>C (p.Gln27Pro) rs2147340525
NM_001356.5(DDX3X):c.869C>T (p.Ser290Leu)
NM_001356.5(DDX3X):c.886C>A (p.Arg296Ser)
NM_001356.5(DDX3X):c.89G>T (p.Gly30Val) rs2147340549
NM_001356.5(DDX3X):c.939G>C (p.Leu313Phe)
NM_001356.5(DDX3X):c.943C>T (p.Arg315Cys)
NM_001356.5(DDX3X):c.959T>C (p.Leu320Ser)
NM_001356.5(DDX3X):c.967A>G (p.Thr323Ala)
NM_001356.5(DDX3X):c.968C>G (p.Thr323Ser)
NM_001356.5(DDX3X):c.998G>A (p.Arg333Lys)

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