ClinVar Miner

List of variants in gene CDC73 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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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.1032T>G (p.Val344=) rs148612206
NM_024529.4(CDC73):c.33C>T (p.Tyr11=) rs150951102
NM_024529.4(CDC73):c.840G>A (p.Leu280=) rs10921320

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