"Genetic Services Laboratory, University of Chicago"[submitter] AND "C - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 128566	NM_015215.4(CAMTA1):c.981C>T (p.Asn327=)	CAMTA1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 434564	NM_015215.4(CAMTA1):c.1015A>G (p.Ser339Gly)	CAMTA1 (S339G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 128564	NM_015215.4(CAMTA1):c.1350G>A (p.Ser450=)	CAMTA1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 434565	NM_015215.4(CAMTA1):c.1441A>G (p.Met481Val)	CAMTA1 (M481V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 210560	NM_015215.4(CAMTA1):c.2568G>A (p.Ser856=)	CAMTA1	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 128565	NM_015215.4(CAMTA1):c.3531C>G (p.Asn1177Lys)	CAMTA1 (N1177K +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign

ClinVar