ClinVar Miner

List of variants in gene CDC73 studied for Hyperparathyroidism 2

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Gene type:
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Total variants: 82
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HGVS dbSNP
CDC73, 2-BP DEL
CDC73, 41-BP DUP/INS
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.*1083A>T rs367704451
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.*1251A>G rs550417983
NM_024529.4(CDC73):c.*1267A>G rs78218016
NM_024529.4(CDC73):c.*12C>A rs193025205
NM_024529.4(CDC73):c.*1303A>G rs886045723
NM_024529.4(CDC73):c.*1365T>C rs180929933
NM_024529.4(CDC73):c.*1472T>G rs576716003
NM_024529.4(CDC73):c.*1499T>A rs138503809
NM_024529.4(CDC73):c.*1599A>G rs543573271
NM_024529.4(CDC73):c.*1761T>C rs528066706
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.*2085G>C rs150030810
NM_024529.4(CDC73):c.*2131A>T rs886045728
NM_024529.4(CDC73):c.*2304T>G rs144363422
NM_024529.4(CDC73):c.*2420A>C rs536960020
NM_024529.4(CDC73):c.*2427T>C rs372585994
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.*2677G>A rs192018514
NM_024529.4(CDC73):c.*2950A>G rs144681513
NM_024529.4(CDC73):c.*2962T>C rs147904515
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.*3266A>G rs532839308
NM_024529.4(CDC73):c.*3409_*3410del rs886045735
NM_024529.4(CDC73):c.*3419T>A rs566373225
NM_024529.4(CDC73):c.*3507G>T rs151216299
NM_024529.4(CDC73):c.*3524A>G rs548190260
NM_024529.4(CDC73):c.*3542A>G rs886045736
NM_024529.4(CDC73):c.*3641G>A rs565579791
NM_024529.4(CDC73):c.*3714T>C rs886045737
NM_024529.4(CDC73):c.*3785A>G rs886045738
NM_024529.4(CDC73):c.*3786T>A rs74130943
NM_024529.4(CDC73):c.*3786T>C rs74130943
NM_024529.4(CDC73):c.*3791T>C rs886045739
NM_024529.4(CDC73):c.*3811_*3813delTTG rs143131672
NM_024529.4(CDC73):c.*453A>C rs547363180
NM_024529.4(CDC73):c.*463A>G rs879039427
NM_024529.4(CDC73):c.*518A>G rs190433473
NM_024529.4(CDC73):c.*580A>T rs191600804
NM_024529.4(CDC73):c.*937G>A rs886045715
NM_024529.4(CDC73):c.*94A>G rs547969893
NM_024529.4(CDC73):c.*956T>C rs886045716
NM_024529.4(CDC73):c.*972A>G rs886045717
NM_024529.4(CDC73):c.-10G>T rs188082584
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.-95G>A rs143969598
NM_024529.4(CDC73):c.1032T>G (p.Val344=) rs148612206
NM_024529.4(CDC73):c.1066+8T>C rs80356647
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.238-1G>A rs587776559
NM_024529.4(CDC73):c.25C>T (p.Arg9Ter) rs121434262
NM_024529.4(CDC73):c.33C>T (p.Tyr11=) rs150951102
NM_024529.4(CDC73):c.3G>A (p.Met1Ile) rs28942098
NM_024529.4(CDC73):c.659T>C (p.Val220Ala) rs886045713
NM_024529.4(CDC73):c.679_680insAG (p.Arg227fs) rs80356649
NM_024529.4(CDC73):c.834C>T (p.Pro278=) rs886045714
NM_024529.4(CDC73):c.840G>A (p.Leu280=) rs10921320

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