"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "MTSS1"[gen - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1695237	NM_014751.6(MTSS1):c.1017G>T (p.Pro339=)	MTSS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2658797	NM_014751.6(MTSS1):c.876G>A (p.Ser292=)	MTSS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2658798	NM_014751.6(MTSS1):c.483G>A (p.Gln161=)	MTSS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3024645	GRCh37/hg19 8q23.3-24.3(chr8:113392581-146364022)x3	LY6E, LY6H +173 more	Copy number gain	not provided	GPathogenic

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