"PreventionGenetics, part of Exact Sciences"[submitter] AND "PICALM"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3057529	NM_007166.4(PICALM):c.1777A>G (p.Met593Val)	PICALM (M492V +3 more)	Single nucleotide variant (missense variant)	PICALM-related disorder	GLikely benign
Select item 403297	NM_007166.4(PICALM):c.1770T>G (p.Ala590=)	PICALM	Single nucleotide variant (synonymous variant)	PICALM-related disorder +2 more	GBenign
Select item 3024905	NM_007166.4(PICALM):c.1231G>C (p.Ala411Pro)	PICALM (A360P +1 more)	Single nucleotide variant (missense variant)	PICALM-related disorder +1 more	GLikely benign
Select item 3040645	NM_007166.4(PICALM):c.585T>C (p.Ala195=)	PICALM	Single nucleotide variant (synonymous variant)	PICALM-related disorder	GLikely benign
Select item 3052585	NM_007166.4(PICALM):c.547-5C>T	PICALM	Single nucleotide variant (intron variant)	PICALM-related disorder	GLikely benign
Select item 403299	NM_007166.4(PICALM):c.522G>A (p.Gln174=)	PICALM	Single nucleotide variant (synonymous variant)	PICALM-related disorder +2 more	GBenign

ClinVar