"PreventionGenetics, part of Exact Sciences"[submitter] AND "MARK3"[ge - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040090	NM_001128918.3(MARK3):c.150A>G (p.Gln50=)	MARK3	Single nucleotide variant (synonymous variant +1 more)	MARK3-related condition	GLikely benign
Select item 3042616	NM_001128918.3(MARK3):c.412+4A>T	MARK3	Single nucleotide variant (intron variant)	MARK3-related condition	GLikely benign
Select item 1321158	NM_001128918.3(MARK3):c.413-4A>G	MARK3	Single nucleotide variant (intron variant)	MARK3-related condition +1 more	GBenign
Select item 3041077	NM_001128918.3(MARK3):c.886G>C (p.Gly296Arg)	MARK3 (G217R +3 more)	Single nucleotide variant (missense variant)	MARK3-related condition	GLikely benign
Select item 3033292	NM_001128918.3(MARK3):c.1293G>A (p.Ala431=)	MARK3	Single nucleotide variant (synonymous variant)	MARK3-related condition	GBenign
Select item 3055758	NM_001128918.3(MARK3):c.1314C>A (p.Thr438=)	MARK3	Single nucleotide variant (synonymous variant)	MARK3-related condition	GBenign
Select item 3056411	NM_001128918.3(MARK3):c.1327A>G (p.Ser443Gly)	MARK3 (S364G +4 more)	Single nucleotide variant (missense variant)	MARK3-related condition	GBenign
Select item 3044255	NM_001128918.3(MARK3):c.1389G>A (p.Lys463=)	MARK3	Single nucleotide variant (synonymous variant)	MARK3-related condition	GBenign
Select item 3040703	NM_001128918.3(MARK3):c.1586+4G>C	MARK3	Single nucleotide variant (intron variant)	MARK3-related condition	GLikely benign
Select item 3043460	NM_001128918.3(MARK3):c.1875T>C (p.Leu625=)	MARK3	Single nucleotide variant (synonymous variant +1 more)	MARK3-related condition	GLikely benign
Select item 3048273	NM_001128918.3(MARK3):c.1896C>T (p.Asn632=)	MARK3	Single nucleotide variant (synonymous variant +1 more)	MARK3-related condition	GLikely benign
Select item 3057300	NM_001128918.3(MARK3):c.2201C>T (p.Ser734Leu)	MARK3 (S640L +6 more)	Single nucleotide variant (missense variant)	MARK3-related condition	GLikely benign