"PreventionGenetics, part of Exact Sciences"[submitter] AND "MSTO1"[ge - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 713032	NM_018116.4(MSTO1):c.489C>G (p.Val163=)	MSTO1	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GLikely benign
Select item 3029796	NM_018116.4(MSTO1):c.648T>G (p.His216Gln)	MSTO1 (H161Q +4 more)	Single nucleotide variant (missense variant +1 more)	MSTO1-related disorder	GUncertain significance
Select item 2170288	NM_018116.4(MSTO1):c.679-7C>T	MSTO1	Single nucleotide variant (intron variant)	MSTO1-related disorder +1 more	GLikely benign
Select item 3046331	NM_018116.4(MSTO1):c.735G>A (p.Ala245=)	MSTO1	Single nucleotide variant (synonymous variant +1 more)	MSTO1-related disorder	GLikely benign
Select item 2632372	NM_018116.4(MSTO1):c.772A>G (p.Ile258Val)	MSTO1 (I203V +4 more)	Single nucleotide variant (missense variant +1 more)	MSTO1-related disorder	GUncertain significance
Select item 2075309	NM_018116.4(MSTO1):c.780C>T (p.Thr260=)	MSTO1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3051196	NM_018116.4(MSTO1):c.804C>T (p.Tyr268=)	MSTO1	Single nucleotide variant (synonymous variant +1 more)	MSTO1-related disorder	GLikely benign
Select item 2101017	NM_018116.4(MSTO1):c.814-4C>T	MSTO1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2067904	NM_018116.4(MSTO1):c.930C>T (p.Pro310=)	MSTO1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign