"Baylor Genetics"[submitter] AND "MALT1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1031680	NM_006785.4(MALT1):c.67G>A (p.Ala23Thr)	LOC130062586, MALT1 +1 more (A23T)	Single nucleotide variant (non-coding transcript variant +1 more)	Combined immunodeficiency due to MALT1 deficiency	GUncertain significance
Select item 1031677	NM_006785.4(MALT1):c.133C>G (p.Leu45Val)	LOC130062586, MALT1 +1 more (L45V)	Single nucleotide variant (non-coding transcript variant +1 more)	Combined immunodeficiency due to MALT1 deficiency	GUncertain significance
Select item 474596	NM_006785.4(MALT1):c.649+9C>T	MALT1	Single nucleotide variant (intron variant)	Combined immunodeficiency due to MALT1 deficiency	GConflicting classifications of pathogenicity
Select item 1031678	NM_006785.4(MALT1):c.1401-15G>T	MALT1	Single nucleotide variant (intron variant)	Combined immunodeficiency due to MALT1 deficiency	GConflicting classifications of pathogenicity
Select item 1030155	NM_006785.4(MALT1):c.2191C>G (p.Leu731Val)	MALT1 (L731V +1 more)	Single nucleotide variant (missense variant)	Combined immunodeficiency due to MALT1 deficiency	GUncertain significance
Select item 1031679	NM_006785.4(MALT1):c.2273A>G (p.His758Arg)	MALT1 (H747R +1 more)	Single nucleotide variant (missense variant)	Combined immunodeficiency due to MALT1 deficiency	GUncertain significance

ClinVar