"Blueprint Genetics"[submitter] AND "HRAS"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 567281	NM_005343.4(HRAS):c.394G>A (p.Asp132Asn)	HRAS, LRRC56 (D132N)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 180851	NM_005343.4(HRAS):c.367C>T (p.Arg123Cys)	HRAS, LRRC56 (R123C)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 40439	NM_005343.4(HRAS):c.277A>G (p.Ile93Val)	HRAS, LRRC56 (I93V)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance FDA Recognized database
Select item 12610	NM_005343.4(HRAS):c.173C>T (p.Thr58Ile)	HRAS, LRRC56 (T58I)	Single nucleotide variant (missense variant +1 more)	Costello syndrome	GPathogenic FDA Recognized database
Select item 12609	NM_005343.4(HRAS):c.64C>A (p.Gln22Lys)	HRAS, LRRC56 (Q22K)	Single nucleotide variant (missense variant +1 more)	Costello syndrome +1 more	GLikely pathogenic
Select item 12613	NM_005343.4(HRAS):c.34G>T (p.Gly12Cys)	HRAS, LRRC56 (G12C)	Single nucleotide variant (missense variant +1 more)	not provided +6 more	GPathogenic
Select item 12602	NM_005343.4(HRAS):c.34G>A (p.Gly12Ser)	HRAS, LRRC56 (G12S)	Single nucleotide variant (missense variant +1 more)	Costello syndrome	GPathogenic FDA Recognized database

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