"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "TBX22"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 368661	NM_001109878.2(TBX22):c.-28G>A	TBX22	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 445911	NM_001109878.2(TBX22):c.176-13C>A	TBX22	Single nucleotide variant (intron variant)	Cleft palate with or without ankyloglossia, X-linked +1 more	GBenign/Likely benign
Select item 2660977	NM_001109878.2(TBX22):c.456T>C (p.Tyr152=)	TBX22	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660978	NM_001109878.2(TBX22):c.697G>A (p.Val233Ile)	TBX22 (V113I +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3067805	NM_001109878.2(TBX22):c.906_907delinsGC (p.Ser303Pro)	TBX22 (S183P +1 more)	Indel (missense variant)	not provided	GUncertain significance
Select item 3024654	GRCh37/hg19 Xq12-28(chrX:67292994-155240074)x3	CPXCR1, MAGEE2 +488 more	Copy number gain	not provided	GPathogenic
Select item 425520	GRCh37/hg19 Xp22.2-q25(chrX:11692290-121187337)x2	BEX4, BEX5 +566 more	Copy number gain	not provided	GUncertain significance

ClinVar