ClinVar Miner

List of variants in gene CDC73 reported by Breakthrough Genomics, Breakthrough Genomics

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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_024529.5(CDC73):c.1155-122C>G rs10921328 0.62038
NM_024529.5(CDC73):c.423+108G>A rs10921318 0.60647
NM_024529.5(CDC73):c.1418-67T>G rs41305084 0.05617
NM_024529.5(CDC73):c.1067-108T>G rs41308389 0.04426
NM_024529.5(CDC73):c.729+61T>A rs79598234 0.02240
NM_024529.5(CDC73):c.1067-86C>T rs41302543 0.01942
NM_024529.5(CDC73):c.*1267A>G rs78218016 0.01764
NM_024529.5(CDC73):c.*2950A>G rs144681513 0.01153
NM_024529.5(CDC73):c.1155-165A>G rs150246947 0.01151
NM_024529.5(CDC73):c.828+29A>T rs138541554 0.01151
NM_024529.5(CDC73):c.1185A>G (p.Gln395=) rs116358657 0.00511
NM_024529.5(CDC73):c.1032T>G (p.Val344=) rs148612206 0.00070
NM_024529.5(CDC73):c.*2420A>C rs536960020 0.00010
NM_024529.5(CDC73):c.132-12T>A rs751268088 0.00001
NC_000001.11:g.193121735C>A rs10737621
NM_024529.5(CDC73):c.*1144dup rs538761780
NM_024529.5(CDC73):c.1154+144A>T rs115158706
NM_024529.5(CDC73):c.1317-114T>A rs3738244
NM_024529.5(CDC73):c.1418-17C>G rs11583414
NM_024529.5(CDC73):c.237+28T>C rs4466634

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