ClinVar Miner

List of variants in gene DCDC2 reported by Eurofins NTD LLC (GA)

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Gene type:
ClinVar version:
Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_016356.5(DCDC2):c.1044C>T (p.Asp348=) rs143313706 0.00286
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.1066G>A (p.Ala356Thr) rs183480366 0.00016
NM_016356.5(DCDC2):c.349-9C>G rs765613994 0.00014
NM_016356.5(DCDC2):c.770G>A (p.Arg257His) rs200233521 0.00010
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.445C>T (p.Leu149Phe) rs200595563 0.00005
NM_016356.5(DCDC2):c.1199G>A (p.Arg400His) rs771591530 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.942del (p.Gly315fs) rs1554144869 0.00002
NM_016356.5(DCDC2):c.1023+9C>T rs1303974976 0.00001
NM_016356.5(DCDC2):c.1024A>T (p.Arg342Trp) rs753636454 0.00001
NM_016356.5(DCDC2):c.1102G>A (p.Gly368Arg) rs752022886 0.00001
NM_016356.5(DCDC2):c.1288G>A (p.Glu430Lys) rs781230955 0.00001
NM_016356.5(DCDC2):c.999T>G (p.Thr333=) rs1561889345 0.00001
NM_016356.5(DCDC2):c.1108A>G (p.Asn370Asp) rs778095991
NM_016356.5(DCDC2):c.1217G>A (p.Gly406Glu) rs1561878667
NM_016356.5(DCDC2):c.1314T>C (p.Ser438=) rs201830443
NM_016356.5(DCDC2):c.1356G>A (p.Arg452=) rs1042335474
NM_016356.5(DCDC2):c.1378C>T (p.Pro460Ser) rs1253412168
NM_016356.5(DCDC2):c.1390G>A (p.Glu464Lys) rs1561877167
NM_016356.5(DCDC2):c.294-2A>G rs1554121105
NM_016356.5(DCDC2):c.383C>G (p.Ser128Ter) rs904520404
NM_016356.5(DCDC2):c.529dup (p.Ile177fs) rs904944428
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.558G>T (p.Arg186Ser) rs748032288
NM_016356.5(DCDC2):c.696G>A (p.Arg232=) rs758802517
NM_016356.5(DCDC2):c.869A>G (p.Lys290Arg) rs1561755265
NM_016356.5(DCDC2):c.923-8C>G rs1313039709
NM_016356.5(DCDC2):c.965G>C (p.Arg322Pro) rs77150627
NM_016356.5(DCDC2):c.970dup (p.Ala324fs) rs774115675

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