List of variants in gene TK2 reported as uncertain significance by GeneDx

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_004614.5(TK2):c.680C>T (p.Pro227Leu)	rs754140768	0.00015
NM_004614.5(TK2):c.620A>T (p.Glu207Val)	rs141225776	0.00007
NM_004614.5(TK2):c.763A>G (p.Ile255Val)	rs144419486	0.00005
NM_004614.5(TK2):c.278A>G (p.Asn93Ser)	rs142291440	0.00004
NM_004614.5(TK2):c.376G>A (p.Val126Met)	rs767386957	0.00003
NM_004614.5(TK2):c.239C>T (p.Thr80Met)	rs750719016	0.00001
NM_004614.5(TK2):c.497A>T (p.Asp166Val)	rs921593414	0.00001
NM_004614.5(TK2):c.755G>A (p.Arg252Gln)	rs772329162	0.00001
NM_004614.5(TK2):c.232G>A (p.Val78Met)	rs1348026323
NM_004614.5(TK2):c.367C>T (p.Arg123Cys)	rs753881948
NM_004614.5(TK2):c.520G>C (p.Val174Leu)	rs149036717
NM_004614.5(TK2):c.547C>A (p.Arg183=)	rs137886900
NM_004614.5(TK2):c.694G>A (p.Val232Ile)	rs576020835
NM_004614.5(TK2):c.754C>T (p.Arg252Trp)	rs373264612
NM_004614.5(TK2):c.761G>T (p.Arg254Leu)
NM_004614.5(TK2):c.782G>T (p.Arg261Leu)	rs780483040

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