ClinVar Miner

List of variants in gene WDPCP reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP
NC_000002.11:g.(?_63711718)_(63720094_?)del
NM_015910.6(WDPCP):c.-227C>G rs376940318
NM_015910.6(WDPCP):c.-301G>A rs886056227
NM_015910.6(WDPCP):c.-322delT rs886056228
NM_015910.7(WDPCP):c.*104A>C rs886056222
NM_015910.7(WDPCP):c.*138_*141GTTT[1] rs886056221
NM_015910.7(WDPCP):c.*446C>T rs566014787
NM_015910.7(WDPCP):c.*541C>G rs532612381
NM_015910.7(WDPCP):c.*582C>G rs184659805
NM_015910.7(WDPCP):c.*586_*587AG[2] rs886056220
NM_015910.7(WDPCP):c.*604_*605del rs886056219
NM_015910.7(WDPCP):c.-108_-106GCG[6] rs563531309
NM_015910.7(WDPCP):c.-109G>C rs886056226
NM_015910.7(WDPCP):c.-113C>A rs192963932
NM_015910.7(WDPCP):c.-188G>C rs187916591
NM_015910.7(WDPCP):c.1079C>T (p.Ser360Leu) rs141011629
NM_015910.7(WDPCP):c.1094A>G (p.Glu365Gly) rs201662623
NM_015910.7(WDPCP):c.1102C>T (p.Arg368Cys) rs769112221
NM_015910.7(WDPCP):c.1166G>A (p.Gly389Asp)
NM_015910.7(WDPCP):c.1310G>T (p.Ser437Ile) rs367727948
NM_015910.7(WDPCP):c.1322T>C (p.Met441Thr) rs886056224
NM_015910.7(WDPCP):c.1333G>C (p.Ala445Pro) rs61734466
NM_015910.7(WDPCP):c.1438G>A (p.Val480Ile) rs201412509
NM_015910.7(WDPCP):c.159G>A (p.Ala53=) rs192196713
NM_015910.7(WDPCP):c.160G>A (p.Asp54Asn) rs200322968
NM_015910.7(WDPCP):c.1706A>T (p.Gln569Leu) rs780342443
NM_015910.7(WDPCP):c.1729T>G (p.Phe577Val) rs141845729
NM_015910.7(WDPCP):c.176T>A (p.Ile59Asn) rs202196322
NM_015910.7(WDPCP):c.1788C>T (p.Asp596=) rs185980830
NM_015910.7(WDPCP):c.1923G>A (p.Leu641=) rs886056223
NM_015910.7(WDPCP):c.1945A>G (p.Met649Val) rs759281211
NM_015910.7(WDPCP):c.208+11T>C rs201607698
NM_015910.7(WDPCP):c.209-1G>A rs767481770
NM_015910.7(WDPCP):c.2113G>T (p.Asp705Tyr) rs200378703
NM_015910.7(WDPCP):c.2159-13T>C rs202221613
NM_015910.7(WDPCP):c.2169G>C (p.Leu723=) rs746225322
NM_015910.7(WDPCP):c.2179G>A (p.Gly727Ser) rs369786224
NM_015910.7(WDPCP):c.254C>T (p.Ser85Leu) rs886056225
NM_015910.7(WDPCP):c.272C>T (p.Thr91Met) rs753130718
NM_015910.7(WDPCP):c.628_629TA[3] (p.Lys211fs) rs769674404
NM_015910.7(WDPCP):c.68C>A (p.Pro23Gln) rs141340867
NM_015910.7(WDPCP):c.75+13C>T rs182759221
NM_015910.7(WDPCP):c.760_786del (p.Pro254_Ala262del) rs774995085
NM_015910.7(WDPCP):c.83A>T (p.Asp28Val) rs144703991
NM_015910.7(WDPCP):c.878C>G (p.Thr293Ser)
NM_015910.7(WDPCP):c.955T>G (p.Tyr319Asp) rs863224771
NM_015910.7(WDPCP):c.985G>A (p.Val329Met) rs199959383

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