List of variants in gene CDC73 reported by Sema4, Sema4

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_024529.5(CDC73):c.33C>T (p.Tyr11=)	rs150951102	0.00094
NM_024529.5(CDC73):c.1031-5C>T	rs746118697	0.00005
NM_024529.5(CDC73):c.1453C>G (p.Leu485Val)	rs761968225	0.00001
NM_024529.5(CDC73):c.1538G>A (p.Arg513Gln)	rs1465509067	0.00001
NM_024529.5(CDC73):c.842G>A (p.Arg281His)	rs762716583	0.00001
NM_024529.5(CDC73):c.1006G>T (p.Ala336Ser)	rs2103178083
NM_024529.5(CDC73):c.1011C>G (p.Ala337=)	rs372567546
NM_024529.5(CDC73):c.1560-4dup	rs761016442
NM_024529.5(CDC73):c.29A>T (p.Gln10Leu)	rs2103111611
NM_024529.5(CDC73):c.475G>A (p.Gly159Ser)	rs1675833045
NM_024529.5(CDC73):c.711C>A (p.Ile237=)	rs2103126478
NM_024529.5(CDC73):c.908-6dup	rs563805986

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