"PreventionGenetics, part of Exact Sciences"[submitter] AND "MAPK3"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3056883	NM_002746.3(MAPK3):c.1017+48G>A	MAPK3	Single nucleotide variant (synonymous variant +1 more)	MAPK3-related disorder	GBenign
Select item 710826	NM_002746.3(MAPK3):c.1008G>A (p.Pro336=)	MAPK3	Single nucleotide variant (synonymous variant)	MAPK3-related disorder +1 more	GBenign/Likely benign
Select item 718814	NM_002746.3(MAPK3):c.967G>A (p.Glu323Lys)	MAPK3 (E279K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3047898	NM_002746.3(MAPK3):c.477C>T (p.Ser159=)	MAPK3	Single nucleotide variant (synonymous variant)	MAPK3-related disorder	GLikely benign
Select item 2630365	NM_002746.3(MAPK3):c.126C>A (p.Tyr42Ter)	MAPK3 (Y42*)	Single nucleotide variant (nonsense)	MAPK3-related disorder	GUncertain significance
Select item 3037690	NM_002746.3(MAPK3):c.69G>A (p.Gly23=)	MAPK3	Single nucleotide variant (synonymous variant)	MAPK3-related disorder	GLikely benign

ClinVar