"PreventionGenetics, part of Exact Sciences"[submitter] AND "GTF3C3"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3037273	NM_012086.5(GTF3C3):c.2524C>G (p.Pro842Ala)	GTF3C3 (P842A)	Single nucleotide variant (missense variant)	GTF3C3-related disorder	GLikely benign
Select item 3038834	NM_012086.5(GTF3C3):c.2069+10C>T	GTF3C3	Single nucleotide variant (intron variant)	GTF3C3-related disorder	GLikely benign
Select item 3049059	NM_012086.5(GTF3C3):c.1920C>G (p.Ser640=)	GTF3C3	Single nucleotide variant (synonymous variant)	GTF3C3-related disorder	GLikely benign
Select item 3038925	NM_012086.5(GTF3C3):c.1854C>T (p.Ser618=)	GTF3C3	Single nucleotide variant (synonymous variant)	GTF3C3-related disorder	GLikely benign
Select item 3033906	NM_012086.5(GTF3C3):c.630G>A (p.Ala210=)	GTF3C3	Single nucleotide variant (synonymous variant)	GTF3C3-related disorder	GLikely benign
Select item 3042047	NM_012086.5(GTF3C3):c.338C>G (p.Pro113Arg)	GTF3C3 (P113R)	Single nucleotide variant (missense variant)	GTF3C3-related disorder	GBenign
Select item 3052057	NM_012086.5(GTF3C3):c.309GGA[8] (p.Glu111_Thr112insGlu)	GTF3C3	Microsatellite (inframe insertion)	GTF3C3-related disorder	GLikely benign
Select item 3057070	NM_012086.5(GTF3C3):c.209A>G (p.Asn70Ser)	GTF3C3 (N70S)	Single nucleotide variant (missense variant)	GTF3C3-related disorder	GBenign

ClinVar