"PreventionGenetics, part of Exact Sciences"[submitter] AND "BAZ1A"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053995	NM_013448.3(BAZ1A):c.4094ATA[1] (p.Asn1366del)	BAZ1A (N1334del +1 more)	Microsatellite (inframe deletion)	BAZ1A-related condition	GLikely benign
Select item 3056971	NM_013448.3(BAZ1A):c.3694G>A (p.Asp1232Asn)	BAZ1A (D1200N +1 more)	Single nucleotide variant (missense variant)	BAZ1A-related condition	GLikely benign
Select item 3043885	NM_013448.3(BAZ1A):c.2717A>G (p.Glu906Gly)	BAZ1A (E874G +1 more)	Single nucleotide variant (missense variant)	BAZ1A-related condition	GLikely benign
Select item 2637042	NM_013448.3(BAZ1A):c.2294T>G (p.Val765Gly)	BAZ1A (V733G +1 more)	Single nucleotide variant (missense variant)	BAZ1A-related condition	GUncertain significance
Select item 3056341	NM_013448.3(BAZ1A):c.2094G>A (p.Thr698=)	BAZ1A	Single nucleotide variant (synonymous variant)	BAZ1A-related condition	GLikely benign
Select item 2636418	NM_013448.3(BAZ1A):c.38A>C (p.Lys13Thr)	BAZ1A, BAZ1A-AS1 (K13T)	Single nucleotide variant (missense variant +1 more)	BAZ1A-related condition	GUncertain significance

ClinVar