ClinVar for MedGen (Select 1681177) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 635783	NM_001085049.3(MRAS):c.212A>G (p.Gln71Arg)	MRAS (Q71R)	Single nucleotide variant (missense variant +1 more)	Noonan syndrome 11	GPathogenic
Select item 635782	NM_001085049.3(MRAS):c.203C>T (p.Thr68Ile)	MRAS (T68I)	Single nucleotide variant (missense variant +1 more)	not provided	GPathogenic/Likely pathogenic
Select item 635781	NM_001085049.3(MRAS):c.68G>T (p.Gly23Val)	MRAS (G23V)	Single nucleotide variant (missense variant +1 more)	Noonan syndrome 11 +1 more	GPathogenic

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