ClinVar Miner

List of variants in gene CDC73 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: 44
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HGVS dbSNP
NM_024529.4(CDC73):c.*1056A>C rs548106852
NM_024529.4(CDC73):c.*1074A>T rs886045718
NM_024529.4(CDC73):c.*1075A>G rs886045719
NM_024529.4(CDC73):c.*1092A>G rs886045720
NM_024529.4(CDC73):c.*1144del rs538761780
NM_024529.4(CDC73):c.*1144dup rs538761780
NM_024529.4(CDC73):c.*1303A>G rs886045723
NM_024529.4(CDC73):c.*1599A>G rs543573271
NM_024529.4(CDC73):c.*1787A>G rs747621423
NM_024529.4(CDC73):c.*1833A>G rs150894778
NM_024529.4(CDC73):c.*1858C>G rs886045724
NM_024529.4(CDC73):c.*1956T>C rs886045725
NM_024529.4(CDC73):c.*1985T>A rs886045726
NM_024529.4(CDC73):c.*2043A>T rs886045727
NM_024529.4(CDC73):c.*2131A>T rs886045728
NM_024529.4(CDC73):c.*2446C>T rs572307472
NM_024529.4(CDC73):c.*2455C>T rs886045729
NM_024529.4(CDC73):c.*2651T>G rs886045730
NM_024529.4(CDC73):c.*2963A>G rs886045731
NM_024529.4(CDC73):c.*2982T>C rs886045732
NM_024529.4(CDC73):c.*3086C>T rs886045733
NM_024529.4(CDC73):c.*3257A>G rs886045734
NM_024529.4(CDC73):c.*3409_*3410del rs886045735
NM_024529.4(CDC73):c.*3542A>G rs886045736
NM_024529.4(CDC73):c.*3714T>C rs886045737
NM_024529.4(CDC73):c.*3785A>G rs886045738
NM_024529.4(CDC73):c.*3791T>C rs886045739
NM_024529.4(CDC73):c.*453A>C rs547363180
NM_024529.4(CDC73):c.*463A>G rs879039427
NM_024529.4(CDC73):c.*937G>A rs886045715
NM_024529.4(CDC73):c.*956T>C rs886045716
NM_024529.4(CDC73):c.*972A>G rs886045717
NM_024529.4(CDC73):c.-121G>A rs886045711
NM_024529.4(CDC73):c.-143G>C rs778446879
NM_024529.4(CDC73):c.-186C>G rs886045710
NM_024529.4(CDC73):c.-190G>C rs886045709
NM_024529.4(CDC73):c.-30C>T rs770313192
NM_024529.4(CDC73):c.-4dup rs545666726
NM_024529.4(CDC73):c.1417+9C>T rs769784756
NM_024529.4(CDC73):c.1418-10C>G rs768713729
NM_024529.4(CDC73):c.156A>G (p.Arg52=) rs886045712
NM_024529.4(CDC73):c.201G>A (p.Val67=) rs752298916
NM_024529.4(CDC73):c.659T>C (p.Val220Ala) rs886045713
NM_024529.4(CDC73):c.834C>T (p.Pro278=) rs886045714

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