ClinVar Miner

List of variants in gene CDC73 reported as likely benign for Parathyroid carcinoma

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Gene type:
ClinVar version:
Total variants: 86
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HGVS dbSNP
NM_024529.4(CDC73):c.*1083A>T rs367704451
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.*1365T>C rs180929933
NM_024529.4(CDC73):c.*1472T>G rs576716003
NM_024529.4(CDC73):c.*1499T>A rs138503809
NM_024529.4(CDC73):c.*1761T>C rs528066706
NM_024529.4(CDC73):c.*2085G>C rs150030810
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.*2677G>A rs192018514
NM_024529.4(CDC73):c.*2950A>G rs144681513
NM_024529.4(CDC73):c.*2962T>C rs147904515
NM_024529.4(CDC73):c.*3266A>G rs532839308
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.*3641G>A rs565579791
NM_024529.4(CDC73):c.*3786T>C rs74130943
NM_024529.4(CDC73):c.*3811_*3813delTTG rs143131672
NM_024529.4(CDC73):c.*518A>G rs190433473
NM_024529.4(CDC73):c.*580A>T rs191600804
NM_024529.4(CDC73):c.*94A>G rs547969893
NM_024529.4(CDC73):c.-10G>T rs188082584
NM_024529.4(CDC73):c.-95G>A rs143969598
NM_024529.4(CDC73):c.1011C>T (p.Ala337=) rs372567546
NM_024529.4(CDC73):c.1030+10T>C rs960030007
NM_024529.4(CDC73):c.1031-10T>C rs370349805
NM_024529.4(CDC73):c.1031-10T>G rs370349805
NM_024529.4(CDC73):c.1031-5C>T rs746118697
NM_024529.4(CDC73):c.1032T>G (p.Val344=) rs148612206
NM_024529.4(CDC73):c.1066+10T>C rs376113810
NM_024529.4(CDC73):c.1066+8T>C rs80356647
NM_024529.4(CDC73):c.1067-4A>G rs749519719
NM_024529.4(CDC73):c.1143A>G (p.Leu381=) rs1384414870
NM_024529.4(CDC73):c.1179G>A (p.Lys393=) rs200738107
NM_024529.4(CDC73):c.1215A>T (p.Ile405=) rs765427308
NM_024529.4(CDC73):c.1266A>G (p.Thr422=) rs1553291034
NM_024529.4(CDC73):c.1332C>T (p.Ala444=) rs1060503808
NM_024529.4(CDC73):c.1368T>C (p.Gly456=) rs1553291416
NM_024529.4(CDC73):c.1374A>G (p.Pro458=) rs1257938148
NM_024529.4(CDC73):c.1417+9C>T rs769784756
NM_024529.4(CDC73):c.1418-10C>G rs768713729
NM_024529.4(CDC73):c.1418-10C>T rs768713729
NM_024529.4(CDC73):c.1453C>T (p.Leu485=) rs761968225
NM_024529.4(CDC73):c.1551A>G (p.Thr517=) rs752668844
NM_024529.4(CDC73):c.1559+7C>A rs542111225
NM_024529.4(CDC73):c.1559+8C>G rs751279026
NM_024529.4(CDC73):c.1572G>A (p.Lys524=) rs988984386
NM_024529.4(CDC73):c.1581G>A (p.Ser527=) rs141013612
NM_024529.4(CDC73):c.174T>C (p.Asp58=) rs1060503806
NM_024529.4(CDC73):c.201G>A (p.Val67=) rs752298916
NM_024529.4(CDC73):c.225C>G (p.Val75=) rs1327944866
NM_024529.4(CDC73):c.228A>G (p.Arg76=) rs978907694
NM_024529.4(CDC73):c.238-3dup rs1553278252
NM_024529.4(CDC73):c.27A>G (p.Arg9=) rs763452834
NM_024529.4(CDC73):c.280C>T (p.Leu94=) rs747811573
NM_024529.4(CDC73):c.307+7A>G rs1553278270
NM_024529.4(CDC73):c.315G>A (p.Ser105=) rs771258964
NM_024529.4(CDC73):c.318A>C (p.Ala106=) rs1415842827
NM_024529.4(CDC73):c.333C>T (p.Ser111=) rs374834265
NM_024529.4(CDC73):c.33C>T (p.Tyr11=) rs150951102
NM_024529.4(CDC73):c.370+9T>A rs1553278822
NM_024529.4(CDC73):c.371-4A>G rs374021222
NM_024529.4(CDC73):c.371-7T>C rs757680253
NM_024529.4(CDC73):c.372C>G (p.Val124=) rs746368285
NM_024529.4(CDC73):c.399A>G (p.Ala133=) rs1553278851
NM_024529.4(CDC73):c.498G>A (p.Gln166=) rs1553279087
NM_024529.4(CDC73):c.501T>C (p.Thr167=) rs200603992
NM_024529.4(CDC73):c.534A>G (p.Ser178=) rs150365980
NM_024529.4(CDC73):c.729+7A>G rs1060503807
NM_024529.4(CDC73):c.730-6T>C rs1060503809
NM_024529.4(CDC73):c.795T>C (p.Pro265=) rs1060503804
NM_024529.4(CDC73):c.840G>A (p.Leu280=) rs10921320
NM_024529.4(CDC73):c.855T>C (p.Pro285=) rs1553280489
NM_024529.4(CDC73):c.873C>T (p.Asn291=) rs149400412
NM_024529.4(CDC73):c.879C>T (p.Tyr293=) rs199551585
NM_024529.4(CDC73):c.908-4G>A rs748472788
NM_024529.4(CDC73):c.908-5C>T rs200475944
NM_024529.4(CDC73):c.908-8T>C rs754598606
NM_024529.4(CDC73):c.908-9T>C rs1060503805
NM_024529.4(CDC73):c.912G>T (p.Thr304=) rs758730118
NM_024529.4(CDC73):c.973-8T>C rs557096653
NM_024529.4(CDC73):c.987C>T (p.Ala329=) rs1037572907

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