"PreventionGenetics, part of Exact Sciences"[submitter] AND "TYROBP"[g - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1547938	NM_003332.4(TYROBP):c.267G>A (p.Ser89=)	TYROBP	Single nucleotide variant (synonymous variant +1 more)	TYROBP-related disorder +1 more	GLikely benign
Select item 501065	NM_003332.4(TYROBP):c.238C>T (p.Arg80Trp)	TYROBP (R80W +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GLikely benign
Select item 196360	NM_003332.4(TYROBP):c.163G>T (p.Val55Leu)	TYROBP (V55L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GBenign
Select item 732760	NM_003332.4(TYROBP):c.46C>T (p.Leu16=)	TYROBP	Single nucleotide variant (synonymous variant +1 more)	TYROBP-related disorder +2 more	GConflicting classifications of pathogenicity

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