"GenomeConnect, ClinGen"[submitter] AND "HRAS"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 40431	NM_005343.4(HRAS):c.81T>C (p.His27=)	HRAS, LRRC56	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GBenign FDA Recognized database
Select item 137556	NM_005343.4(HRAS):c.-10C>T	HRAS, LRRC56	Single nucleotide variant (5 prime UTR variant)	not provided +3 more	GBenign
Select item 1339886	GRCh37/hg19 11p15.5-15.4(chr11:230615-5525355)x3	ANO9, AP2A2 +137 more	Copy number gain	not provided	Gnot provided

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