List of variants in gene CDC73 reported as likely benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_024529.5(CDC73):c.*12C>A	rs193025205	0.00196
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.424-16C>T	rs201012067	0.00020
NM_024529.5(CDC73):c.1067-23A>T	rs750567180	0.00008
NM_024529.5(CDC73):c.1154+20A>C	rs567786660	0.00004
NM_024529.5(CDC73):c.534A>G (p.Ser178=)	rs150365980	0.00001
NM_024529.5(CDC73):c.78C>T (p.Ile26=)	rs1675465371	0.00001
NM_024529.5(CDC73):c.-29C>T
NM_024529.5(CDC73):c.-4del	rs545666726
NM_024529.5(CDC73):c.-4dup	rs545666726
NM_024529.5(CDC73):c.1141C>T (p.Leu381=)
NM_024529.5(CDC73):c.1560-16A>T	rs935733228
NM_024529.5(CDC73):c.1560-37C>G
NM_024529.5(CDC73):c.238-31T>A
NM_024529.5(CDC73):c.307+42G>A
NM_024529.5(CDC73):c.412C>A (p.Pro138Thr)	rs369542555
NM_024529.5(CDC73):c.512+35T>C
NM_024529.5(CDC73):c.729+33GA[10]
NM_024529.5(CDC73):c.804A>G (p.Arg268=)	rs2103130595
NM_024529.5(CDC73):c.908-21_908-19del

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