ClinVar Miner

List of variants in gene CDC73 reported as benign for adenocarcinoma

Included ClinVar conditions (112):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_024529.5(CDC73):c.*1267A>G rs78218016 0.01764
NM_024529.5(CDC73):c.*580A>T rs191600804 0.01264
NM_024529.5(CDC73):c.*2950A>G rs144681513 0.01153
NM_024529.5(CDC73):c.*3507G>T rs151216299 0.01140
NM_024529.5(CDC73):c.1185A>G (p.Gln395=) rs116358657 0.00511
NM_024529.5(CDC73):c.*2304T>G rs144363422 0.00424
NM_024529.5(CDC73):c.308-16C>A rs201766013 0.00252
NM_024529.5(CDC73):c.*2085G>C rs150030810 0.00217
NM_024529.5(CDC73):c.*12C>A rs193025205 0.00196
NM_024529.5(CDC73):c.*518A>G rs190433473 0.00195
NM_024529.5(CDC73):c.-95G>A rs143969598 0.00133
NM_024529.5(CDC73):c.33C>T (p.Tyr11=) rs150951102 0.00094
NM_024529.5(CDC73):c.*3524A>G rs548190260 0.00071
NM_024529.5(CDC73):c.1032T>G (p.Val344=) rs148612206 0.00070
NM_024529.5(CDC73):c.-11G>A rs80356643 0.00056
NM_024529.5(CDC73):c.513-17A>C rs202192473 0.00046
NM_024529.5(CDC73):c.873C>T (p.Asn291=) rs149400412 0.00036
NM_024529.5(CDC73):c.-10G>T rs188082584 0.00024
NM_024529.5(CDC73):c.1066+13A>G rs142414871 0.00023
NM_024529.5(CDC73):c.424-16C>T rs201012067 0.00020
NM_024529.5(CDC73):c.*1833A>G rs150894778 0.00018
NM_024529.5(CDC73):c.*2427T>C rs372585994 0.00013
NM_024529.5(CDC73):c.*2677G>A rs192018514 0.00010
NM_024529.5(CDC73):c.*1499T>A rs138503809 0.00009
NM_024529.5(CDC73):c.1154+18C>G rs145348897 0.00008
NM_024529.5(CDC73):c.*1083A>T rs367704451 0.00006
NM_024529.5(CDC73):c.450A>G (p.Lys150=) rs779144943 0.00002
NM_024529.5(CDC73):c.*3063G>A rs182545034 0.00001
NM_024529.5(CDC73):c.*3786T>A rs74130943
NM_024529.5(CDC73):c.*3786T>C rs74130943
NM_024529.5(CDC73):c.-4dup rs545666726
NM_024529.5(CDC73):c.1031-12del rs751580604
NM_024529.5(CDC73):c.1031-12dup rs751580604
NM_024529.5(CDC73):c.1155-6dup
NM_024529.5(CDC73):c.1418-17C>G rs11583414
NM_024529.5(CDC73):c.1560-4del
NM_024529.5(CDC73):c.1560-4dup rs761016442
NM_024529.5(CDC73):c.308-11del
NM_024529.5(CDC73):c.829-5dup rs755393679
NM_024529.5(CDC73):c.908-6dup rs563805986

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