"Invitae"[submitter] AND "TBX22"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 368664	NM_001109878.2(TBX22):c.72C>T (p.Leu24=)	TBX22	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 736301	NM_001109878.2(TBX22):c.176-9G>A	TBX22	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 726731	NM_001109878.2(TBX22):c.702C>T (p.Asp234=)	TBX22	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 753761	NM_001109878.2(TBX22):c.780G>A (p.Thr260=)	TBX22	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 729592	NM_001109878.2(TBX22):c.804G>A (p.Thr268=)	TBX22	Single nucleotide variant (synonymous variant)	TBX22-related condition +2 more	GBenign/Likely benign
Select item 738652	NM_001109878.2(TBX22):c.930C>A (p.Thr310=)	TBX22	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 723460	NM_001109878.2(TBX22):c.936C>T (p.Gly312=)	TBX22	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 780710	NM_001109878.2(TBX22):c.1090C>T (p.Leu364=)	TBX22	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 742205	NM_001109878.2(TBX22):c.1212C>T (p.Ala404=)	TBX22	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 752846	NM_001109878.2(TBX22):c.1377C>A (p.Ile459=)	TBX22	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 755941	NM_001109878.2(TBX22):c.1424A>T (p.Tyr475Phe)	TBX22 (Y355F +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 713489	NM_001109878.2(TBX22):c.1488C>T (p.Asp496=)	TBX22	Single nucleotide variant (synonymous variant)	Cleft palate with or without ankyloglossia, X-linked +2 more	GConflicting classifications of pathogenicity