"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZSCAN29"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3057565	NM_001372080.1(ZSCAN29):c.2509G>A (p.Gly837Arg)	ZSCAN29 (G837R)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 3039844	NM_001372080.1(ZSCAN29):c.2427T>C (p.His809=)	ZSCAN29	Single nucleotide variant (synonymous variant)	ZSCAN29-related disorder	GLikely benign
Select item 3060359	NM_001372080.1(ZSCAN29):c.2181C>T (p.Ile727=)	ZSCAN29	Single nucleotide variant (synonymous variant)	ZSCAN29-related disorder	GBenign
Select item 3042865	NM_001372080.1(ZSCAN29):c.1979T>G (p.Phe660Cys)	ZSCAN29 (F660C)	Single nucleotide variant (missense variant)	ZSCAN29-related disorder	GLikely benign
Select item 3050824	NM_001372080.1(ZSCAN29):c.1950C>T (p.Pro650=)	ZSCAN29	Single nucleotide variant (synonymous variant)	ZSCAN29-related disorder	GLikely benign
Select item 3038810	NM_001372080.1(ZSCAN29):c.1109AGG[1] (p.Glu371del)	ZSCAN29 (E371del)	Microsatellite (inframe deletion)	ZSCAN29-related disorder	GBenign
Select item 3052663	NM_001372080.1(ZSCAN29):c.408G>A (p.Glu136=)	ZSCAN29	Single nucleotide variant (synonymous variant)	ZSCAN29-related disorder	GLikely benign
Select item 3046552	NM_001372080.1(ZSCAN29):c.228T>C (p.Asn76=)	ZSCAN29	Single nucleotide variant (synonymous variant)	ZSCAN29-related disorder	GLikely benign

ClinVar