List of variants in gene PLK4 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_014264.5(PLK4):c.950C>T (p.Pro317Leu)	rs35049837	0.00228
NM_014264.5(PLK4):c.618C>T (p.Ile206=)	rs199907384	0.00012
NM_014264.5(PLK4):c.162A>G (p.Val54=)	rs199771668	0.00006
NM_014264.5(PLK4):c.1011A>G (p.Ser337=)	rs201311086	0.00001
NM_014264.5(PLK4):c.1312T>C (p.Ser438Pro)	rs751170471	0.00001
NM_014264.5(PLK4):c.1857G>A (p.Val619=)	rs761842515
NM_014264.5(PLK4):c.2070C>T (p.Ser690=)
NM_014264.5(PLK4):c.303A>G (p.Leu101=)
NM_014264.5(PLK4):c.567C>T (p.Gly189=)

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