"Women's Health and Genetics/Laboratory Corporation of America, LabCor - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1029370	NM_015215.4(CAMTA1):c.718G>A (p.Val240Met)	CAMTA1 (V240M +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1878235	NM_015215.4(CAMTA1):c.2290C>T (p.His764Tyr)	CAMTA1 (H740Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2445746	NM_015215.4(CAMTA1):c.2614A>G (p.Met872Val)	CAMTA1 (M842V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2637701	NM_015215.4(CAMTA1):c.3658+13A>G	CAMTA1	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 2682292	NM_015215.4(CAMTA1):c.4307C>T (p.Thr1436Ile)	CAMTA1 (T1293I +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1723241	NM_015215.4(CAMTA1):c.4982A>G (p.Tyr1661Cys)	CAMTA1 (Y1525C +7 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2627295	NC_000001.10:g.(7309687_7527889)_(7527962_7700459)dup	CAMTA1	Duplication	not specified	GUncertain significance

ClinVar