List of variants in gene TG 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_003235.5(TG):c.6181G>A (p.Gly2061Arg)	rs115436575	0.00198
NM_003235.5(TG):c.4481C>T (p.Pro1494Leu)	rs146498231	0.00052
NM_003235.5(TG):c.3139+9G>A	rs201582196	0.00048
NM_003235.5(TG):c.4378G>A (p.Val1460Ile)	rs199615848	0.00019
NM_003235.5(TG):c.4268G>A (p.Arg1423His)	rs146594373	0.00013
NM_003235.5(TG):c.4990G>A (p.Val1664Met)	rs180705321	0.00011
NM_003235.5(TG):c.3149G>T (p.Trp1050Leu)	rs142124591	0.00007
NM_003235.5(TG):c.6707C>T (p.Pro2236Leu)	rs145564745	0.00002
NM_003235.5(TG):c.1775C>T (p.Ala592Val)
NM_003235.5(TG):c.1890A>T (p.Gln630His)
NM_003235.5(TG):c.3727C>G (p.Gln1243Glu)
NM_003235.5(TG):c.3836G>A (p.Arg1279Gln)
NM_003235.5(TG):c.4474C>T (p.Pro1492Ser)
NM_003235.5(TG):c.506GTC[1] (p.Arg170del)	rs2132059579
NM_003235.5(TG):c.5447A>G (p.Gln1816Arg)
NM_003235.5(TG):c.6397G>C (p.Glu2133Gln)
NM_003235.5(TG):c.6619G>A (p.Gly2207Ser)
NM_003235.5(TG):c.6783-8A>G	rs780817859
NM_003235.5(TG):c.7165G>C (p.Ala2389Pro)	rs765477121

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