List of variants in gene TGFB2 reported 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
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_003238.6(TGFB2):c.1239C>T (p.Cys413=)	rs141225367	0.00359
NM_003238.6(TGFB2):c.619G>C (p.Val207Leu)	rs10482810	0.00359
NM_003238.6(TGFB2):c.272G>A (p.Arg91His)	rs10482721	0.00297
NM_003238.6(TGFB2):c.114G>A (p.Glu38=)	rs149215818	0.00087
NM_003238.6(TGFB2):c.303G>A (p.Lys101=)	rs147052890	0.00072
NM_003238.6(TGFB2):c.356C>T (p.Pro119Leu)	rs149533093	0.00047
NM_003238.6(TGFB2):c.1053G>A (p.Pro351=)	rs142741166	0.00004
NM_003238.6(TGFB2):c.1181T>C (p.Ile394Thr)	rs886045980	0.00001
NM_003238.6(TGFB2):c.548G>A (p.Arg183His)	rs773177511	0.00001
NM_003238.6(TGFB2):c.1139G>A (p.Cys380Tyr)	rs1553303745
NM_003238.6(TGFB2):c.245C>T (p.Ala82Val)	rs1571821016
NM_003238.6(TGFB2):c.414G>C (p.Glu138Asp)	rs2102594828
NM_003238.6(TGFB2):c.635del (p.His212fs)
NM_003238.6(TGFB2):c.895C>T (p.Arg299Trp)	rs863223792

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