"PreventionGenetics, part of Exact Sciences"[submitter] AND "TFAP2B"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3037790	NM_003221.4(TFAP2B):c.117G>A (p.Arg39=)	TFAP2B	Single nucleotide variant (synonymous variant)	TFAP2B-related disorder	GLikely benign
Select item 258985	NM_003221.4(TFAP2B):c.540+7ACAA[5]	TFAP2B	Microsatellite (intron variant)	not specified +2 more	GBenign
Select item 258984	NM_003221.4(TFAP2B):c.540+10A>G	TFAP2B	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2629413	NM_003221.4(TFAP2B):c.1267G>C (p.Glu423Gln)	TFAP2B (E423Q)	Single nucleotide variant (missense variant)	TFAP2B-related disorder	GUncertain significance
Select item 357286	NM_003221.4(TFAP2B):c.1304A>C (p.Asn435Thr)	TFAP2B (N435T)	Single nucleotide variant (missense variant)	TFAP2B-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 258983	NM_003221.4(TFAP2B):c.*10A>T	TFAP2B	Single nucleotide variant (3 prime UTR variant)	not specified +1 more	GBenign

ClinVar