List of variants in gene TGFB1 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000660.7(TGFB1):c.466C>T (p.Arg156Cys)	rs200482214	0.00003
NM_000660.7(TGFB1):c.1153C>G (p.Arg385Gly)	rs981119783	0.00002
NM_000660.7(TGFB1):c.1159T>G (p.Cys387Gly)	rs1336387628	0.00001
NM_000660.7(TGFB1):c.899T>C (p.Ile300Thr)	rs201635147	0.00001
NM_000660.7(TGFB1):c.1030A>T (p.Asn344Tyr)
NM_000660.7(TGFB1):c.1031A>C (p.Asn344Thr)	rs2123077879
NM_000660.7(TGFB1):c.1138T>C (p.Ser380Pro)
NM_000660.7(TGFB1):c.1161dup (p.Lys388fs)	rs2513371745
NM_000660.7(TGFB1):c.360C>G (p.Ile120Met)	rs1018687476
NM_000660.7(TGFB1):c.553C>T (p.Arg185Trp)	rs201055697
NM_000660.7(TGFB1):c.570C>G (p.Ser190Arg)	rs779809888
NM_000660.7(TGFB1):c.786_791delinsTGCTTCACCAT (p.Thr263fs)	rs2513381200
NM_000660.7(TGFB1):c.829C>T (p.Arg277Cys)	rs1274564517
NM_000660.7(TGFB1):c.86G>A (p.Gly29Glu)	rs199758510
NM_000660.7(TGFB1):c.949T>C (p.Tyr317His)

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