ClinVar Miner

List of variants in gene DDX41 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_016222.4(DDX41):c.6G>T (p.Glu2Asp) rs138435584 0.00032
NM_016222.4(DDX41):c.465G>A (p.Met155Ile) rs199697328 0.00031
NM_016222.4(DDX41):c.97T>C (p.Tyr33His) rs150205465 0.00023
NM_016222.4(DDX41):c.38C>T (p.Thr13Ile) rs61736559 0.00010
NM_016222.4(DDX41):c.*63T>C rs937006672 0.00009
NM_016222.4(DDX41):c.88G>T (p.Asp30Tyr) rs559527781 0.00008
NM_016222.4(DDX41):c.1016G>A (p.Arg339His) rs774698335 0.00006
NM_016222.4(DDX41):c.1622-3C>T rs200471726 0.00004
NM_016222.4(DDX41):c.1547A>G (p.Tyr516Cys) rs1014402897 0.00003
NM_016222.4(DDX41):c.560A>G (p.Lys187Arg) rs185950985 0.00003
NM_016222.4(DDX41):c.*194A>G rs750795230 0.00002
NM_016222.4(DDX41):c.653G>A (p.Gly218Asp) rs371460149 0.00002
NM_016222.4(DDX41):c.766G>A (p.Glu256Lys) rs746011550 0.00002
NM_016222.4(DDX41):c.*181C>G rs867695519 0.00001
NM_016222.4(DDX41):c.1033G>A (p.Glu345Lys) rs370129260 0.00001
NM_016222.4(DDX41):c.1079C>T (p.Thr360Ile) rs1284223764 0.00001
NM_016222.4(DDX41):c.1458A>G (p.Leu486=) rs1481876340 0.00001
NM_016222.4(DDX41):c.1650G>A (p.Ala550=) rs747056004 0.00001
NM_016222.4(DDX41):c.1665C>T (p.Ala555=) rs1356103698 0.00001
NM_016222.4(DDX41):c.198C>A (p.Ser66Arg) rs1231474960 0.00001
NM_016222.4(DDX41):c.511G>C (p.Val171Leu) rs200005940 0.00001
NM_016222.4(DDX41):c.566C>T (p.Pro189Leu) rs776934246 0.00001
NM_016222.4(DDX41):c.645-10C>T rs780120166 0.00001
NM_016222.4(DDX41):c.877C>T (p.Arg293Cys) rs763133277 0.00001
NM_016222.4(DDX41):c.1013G>A (p.Cys338Tyr) rs148384288
NM_016222.4(DDX41):c.1105C>G (p.Arg369Gly) rs747672157
NM_016222.4(DDX41):c.1283T>C (p.Leu428Pro) rs1761050435
NM_016222.4(DDX41):c.1332C>T (p.Asp444=) rs554494724
NM_016222.4(DDX41):c.138+5G>A rs187714514
NM_016222.4(DDX41):c.138+5G>T rs187714514
NM_016222.4(DDX41):c.157C>G (p.Arg53Gly) rs745421135
NM_016222.4(DDX41):c.27+9G>A rs765022870
NM_016222.4(DDX41):c.299-3C>T rs758614565
NM_016222.4(DDX41):c.301C>T (p.Arg101Cys) rs1761223083
NM_016222.4(DDX41):c.5A>C (p.Glu2Ala) rs1399847240
NM_016222.4(DDX41):c.616C>G (p.Pro206Ala)
NM_016222.4(DDX41):c.681G>C (p.Thr227=) rs765996540
NM_016222.4(DDX41):c.920T>C (p.Met307Thr)
NM_016222.4(DDX41):c.926C>T (p.Thr309Ile) rs371035635
NM_016222.4(DDX41):c.959C>T (p.Thr320Ile) rs2127436611

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