ClinVar Miner

List of variants in gene DCDC2 studied for biliary tract disorder

Included ClinVar conditions (55):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 128
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HGVS dbSNP gnomAD frequency
NM_016356.5(DCDC2):c.426-13C>T rs807703 0.98337
NM_016356.5(DCDC2):c.*3C>G rs9358755 0.72045
NM_016356.5(DCDC2):c.661A>G (p.Ser221Gly) rs2274305 0.51051
NM_016356.5(DCDC2):c.1368A>T (p.Lys456Asn) rs9460973 0.15425
NM_016356.5(DCDC2):c.1017C>T (p.Val339=) rs9467075 0.13584
NM_016356.5(DCDC2):c.454C>G (p.Pro152Ala) rs33914824 0.03882
NM_016356.5(DCDC2):c.1044C>T (p.Asp348=) rs143313706 0.00286
NM_016356.5(DCDC2):c.425+14C>A rs77544788 0.00279
NM_016356.5(DCDC2):c.855A>G (p.Ser285=) rs141519329 0.00249
NM_016356.5(DCDC2):c.1208G>A (p.Arg403His) rs139858268 0.00194
NM_016356.5(DCDC2):c.715T>G (p.Ser239Ala) rs144695853 0.00183
NM_016356.5(DCDC2):c.402G>A (p.Pro134=) rs142088541 0.00064
NM_016356.5(DCDC2):c.1423G>A (p.Val475Met) rs145154884 0.00062
NM_016356.5(DCDC2):c.817C>T (p.Pro273Ser) rs146787541 0.00061
NM_016356.5(DCDC2):c.478A>C (p.Arg160=) rs201204772 0.00030
NM_016356.5(DCDC2):c.888A>G (p.Lys296=) rs41271773 0.00029
NM_016356.5(DCDC2):c.349-15C>T rs200146922 0.00025
NM_016356.5(DCDC2):c.1066G>A (p.Ala356Thr) rs183480366 0.00016
NM_016356.5(DCDC2):c.923-12T>G rs200973005 0.00015
NM_016356.5(DCDC2):c.349-9C>G rs765613994 0.00014
NM_016356.5(DCDC2):c.750T>G (p.Ser250=) rs372157851 0.00011
NM_016356.5(DCDC2):c.785C>T (p.Thr262Ile) rs200534758 0.00011
NM_016356.5(DCDC2):c.1422C>T (p.Ala474=) rs146868469 0.00010
NM_016356.5(DCDC2):c.770G>A (p.Arg257His) rs200233521 0.00010
NM_016356.5(DCDC2):c.705-4A>C rs774040286 0.00007
NM_016356.5(DCDC2):c.954G>A (p.Arg318=) rs140084657 0.00007
NM_016356.5(DCDC2):c.355C>T (p.Pro119Ser) rs1056029060 0.00006
NM_016356.5(DCDC2):c.349G>A (p.Val117Ile) rs781510673 0.00005
NM_016356.5(DCDC2):c.445C>T (p.Leu149Phe) rs200595563 0.00005
NM_016356.5(DCDC2):c.1199G>A (p.Arg400His) rs771591530 0.00004
NM_016356.5(DCDC2):c.1203T>A (p.Pro401=) rs143452599 0.00004
NM_016356.5(DCDC2):c.1237G>A (p.Gly413Ser) rs771499861 0.00004
NM_016356.5(DCDC2):c.1344A>G (p.Gln448=) rs368603558 0.00004
NM_016356.5(DCDC2):c.1100C>T (p.Ser367Leu) rs757670255 0.00003
NM_016356.5(DCDC2):c.1359A>G (p.Pro453=) rs374448795 0.00003
NM_016356.5(DCDC2):c.1364T>C (p.Val455Ala) rs763350514 0.00003
NM_016356.5(DCDC2):c.349-2A>G rs760040426 0.00003
NM_016356.5(DCDC2):c.769C>T (p.Arg257Cys) rs909339162 0.00003
NM_016356.5(DCDC2):c.1071C>A (p.Asn357Lys) rs746347880 0.00002
NM_016356.5(DCDC2):c.1099T>A (p.Ser367Thr) rs538198742 0.00002
NM_016356.5(DCDC2):c.1154C>T (p.Pro385Leu) rs773020868 0.00002
NM_016356.5(DCDC2):c.456A>G (p.Pro152=) rs764454438 0.00002
NM_016356.5(DCDC2):c.685A>G (p.Thr229Ala) rs1043649931 0.00002
NM_016356.5(DCDC2):c.942del (p.Gly315fs) rs1554144869 0.00002
NM_016356.5(DCDC2):c.1024A>T (p.Arg342Trp) rs753636454 0.00001
NM_016356.5(DCDC2):c.1223C>T (p.Thr408Ile) rs1367144327 0.00001
NM_016356.5(DCDC2):c.1241A>C (p.Glu414Ala) rs773832570 0.00001
NM_016356.5(DCDC2):c.401C>T (p.Pro134Leu) rs779076957 0.00001
NM_016356.5(DCDC2):c.471T>G (p.Leu157=) rs374456364 0.00001
NM_016356.5(DCDC2):c.890T>A (p.Leu297Ter) rs1050411259 0.00001
NM_016356.5(DCDC2):c.923-18G>A rs768651764 0.00001
NM_016356.5(DCDC2):c.929G>C (p.Gly310Ala) rs746447569 0.00001
NM_016356.5(DCDC2):c.999T>G (p.Thr333=) rs1561889345 0.00001
NC_000006.11:g.(?_24174958)_(24178880_?)dup
NM_016356.4(DCDC2):c.426_557del
NM_016356.5(DCDC2):c.1023+11T>C
NM_016356.5(DCDC2):c.1023+14C>A
NM_016356.5(DCDC2):c.1024-16C>T
NM_016356.5(DCDC2):c.1056T>G (p.Asp352Glu)
NM_016356.5(DCDC2):c.1076A>T (p.Asp359Val) rs1393437679
NM_016356.5(DCDC2):c.1164C>T (p.Val388=) rs767129413
NM_016356.5(DCDC2):c.1165G>A (p.Glu389Lys)
NM_016356.5(DCDC2):c.1207C>T (p.Arg403Cys)
NM_016356.5(DCDC2):c.1219G>C (p.Gly407Arg) rs756047736
NM_016356.5(DCDC2):c.1220G>T (p.Gly407Val)
NM_016356.5(DCDC2):c.1221C>G (p.Gly407=)
NM_016356.5(DCDC2):c.1224C>A (p.Thr408=) rs763861048
NM_016356.5(DCDC2):c.1224C>T (p.Thr408=)
NM_016356.5(DCDC2):c.1272A>G (p.Gln424=)
NM_016356.5(DCDC2):c.1275G>T (p.Leu425=)
NM_016356.5(DCDC2):c.1283A>T (p.Asp428Val) rs375119774
NM_016356.5(DCDC2):c.1313G>T (p.Ser438Ile)
NM_016356.5(DCDC2):c.1318C>T (p.Gln440Ter)
NM_016356.5(DCDC2):c.1326+9A>G
NM_016356.5(DCDC2):c.1327-15T>A
NM_016356.5(DCDC2):c.1406A>C (p.Asn469Thr)
NM_016356.5(DCDC2):c.294-11T>A
NM_016356.5(DCDC2):c.294-21GTTT[2] rs374485384
NM_016356.5(DCDC2):c.326C>T (p.Pro109Leu)
NM_016356.5(DCDC2):c.349-16dup rs746353912
NM_016356.5(DCDC2):c.349-8T>G
NM_016356.5(DCDC2):c.366T>C (p.His122=)
NM_016356.5(DCDC2):c.383C>G (p.Ser128Ter) rs904520404
NM_016356.5(DCDC2):c.388C>T (p.Arg130Cys)
NM_016356.5(DCDC2):c.425+11A>T
NM_016356.5(DCDC2):c.426-2A>G rs2113838226
NM_016356.5(DCDC2):c.463C>T (p.Arg155Cys)
NM_016356.5(DCDC2):c.467T>A (p.Leu156His)
NM_016356.5(DCDC2):c.529dup (p.Ile177fs) rs904944428
NM_016356.5(DCDC2):c.536_537del (p.Leu179fs) rs2113838075
NM_016356.5(DCDC2):c.543C>A (p.Ser181Arg) rs141060456
NM_016356.5(DCDC2):c.543C>T (p.Ser181=) rs141060456
NM_016356.5(DCDC2):c.549dup (p.Val184fs) rs1581640646
NM_016356.5(DCDC2):c.555C>T (p.His185=)
NM_016356.5(DCDC2):c.557+14A>G
NM_016356.5(DCDC2):c.558-4A>G
NM_016356.5(DCDC2):c.558-5G>T
NM_016356.5(DCDC2):c.558-6C>T
NM_016356.5(DCDC2):c.649A>T (p.Lys217Ter) rs730880299
NM_016356.5(DCDC2):c.656C>T (p.Pro219Leu)
NM_016356.5(DCDC2):c.660_661inv (p.Ser221Gly)
NM_016356.5(DCDC2):c.662G>A (p.Ser221Asn)
NM_016356.5(DCDC2):c.690G>A (p.Met230Ile)
NM_016356.5(DCDC2):c.696G>A (p.Arg232=) rs758802517
NM_016356.5(DCDC2):c.696G>T (p.Arg232Ser)
NM_016356.5(DCDC2):c.705-10G>T rs1554116524
NM_016356.5(DCDC2):c.705-11del rs758628136
NM_016356.5(DCDC2):c.705-2A>G
NM_016356.5(DCDC2):c.728C>G (p.Pro243Arg) rs948355469
NM_016356.5(DCDC2):c.732T>C (p.Ile244=)
NM_016356.5(DCDC2):c.755G>C (p.Gly252Ala)
NM_016356.5(DCDC2):c.759+17T>G
NM_016356.5(DCDC2):c.760-7C>T
NM_016356.5(DCDC2):c.802A>G (p.Asn268Asp) rs1438044739
NM_016356.5(DCDC2):c.803A>G (p.Asn268Ser)
NM_016356.5(DCDC2):c.840AGA[1] (p.Glu281del) rs760375899
NM_016356.5(DCDC2):c.866C>T (p.Thr289Met)
NM_016356.5(DCDC2):c.886A>G (p.Lys296Glu)
NM_016356.5(DCDC2):c.918T>C (p.Asn306=) rs1239033952
NM_016356.5(DCDC2):c.922+19T>C
NM_016356.5(DCDC2):c.923-10G>T
NM_016356.5(DCDC2):c.923-12_923-9del
NM_016356.5(DCDC2):c.923-283_1023+141del rs1761673797
NM_016356.5(DCDC2):c.923-8C>T
NM_016356.5(DCDC2):c.965G>C (p.Arg322Pro) rs77150627
NM_016356.5(DCDC2):c.970G>T (p.Ala324Ser) rs1416369642
NM_016356.5(DCDC2):c.970dup (p.Ala324fs) rs774115675
NM_016356.5(DCDC2):c.992A>T (p.Glu331Val)

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