"ITMI"[submitter] AND "SMARCB1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 135257	NM_003073.5(SMARCB1):c.1A>G (p.Met1Val)	SMARCB1 (M1V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 41778	NM_003073.5(SMARCB1):c.500+24C>G	SMARCB1 (T166S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 133387	NM_003073.5(SMARCB1):c.500+41G>A	SMARCB1 (A172T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 133388	NM_003073.5(SMARCB1):c.500+65G>A	SMARCB1	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 133389	NM_003073.5(SMARCB1):c.500+111C>A	SMARCB1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 133390	NM_003073.5(SMARCB1):c.500+114A>G	SMARCB1	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133391	NM_003073.5(SMARCB1):c.500+116C>T	SMARCB1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 133392	NM_003073.5(SMARCB1):c.500+234C>G	SMARCB1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 133393	NM_003073.5(SMARCB1):c.500+305C>A	SMARCB1	Single nucleotide variant (intron variant)	not provided	GLikely benign

ClinVar