List of variants in gene TFG reported as uncertain significance 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_006070.6(TFG):c.1147C>T (p.Arg383Cys)	rs146078119	0.00006
NM_006070.6(TFG):c.545T>C (p.Met182Thr)	rs199724547	0.00006
NM_006070.6(TFG):c.944C>T (p.Pro315Leu)	rs753375115	0.00006
NM_006070.6(TFG):c.771G>A (p.Gln257=)	rs374006808	0.00002
NM_006070.6(TFG):c.550G>A (p.Ala184Thr)	rs777654574	0.00001
NM_006070.6(TFG):c.1056C>T (p.Ser352=)	rs2149106566
NM_006070.6(TFG):c.1132C>G (p.Pro378Ala)
NM_006070.6(TFG):c.320G>A (p.Arg107Gln)
NM_006070.6(TFG):c.341A>G (p.Asn114Ser)	rs752292956
NM_006070.6(TFG):c.37A>G (p.Ile13Val)	rs200695895
NM_006070.6(TFG):c.562A>G (p.Thr188Ala)
NM_006070.6(TFG):c.931C>T (p.Leu311=)

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