List of variants in gene CDC14A reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_003672.4(CDC14A):c.990G>A (p.Ser330=)	rs2270694	0.11151
NM_003672.4(CDC14A):c.309A>C (p.Ala103=)	rs28361212	0.09875
NM_003672.4(CDC14A):c.825C>T (p.Ala275=)	rs7543221	0.06126
NM_003672.4(CDC14A):c.903T>C (p.His301=)	rs17122597	0.05859
NM_003672.4(CDC14A):c.1647C>T (p.Ser549=)	rs35385659	0.01241
NM_003672.4(CDC14A):c.608-10G>A	rs114626664	0.00462
NM_003672.4(CDC14A):c.1755+8C>T	rs139956023	0.00461
NM_003672.4(CDC14A):c.819C>G (p.Ala273=)	rs28364884	0.00453
NM_003672.4(CDC14A):c.1711G>A (p.Gly571Arg)	rs61752469	0.00224
NM_003672.4(CDC14A):c.822C>T (p.Ile274=)	rs74667145	0.00158
NM_003672.4(CDC14A):c.1755+110C>G	rs188557928	0.00016

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