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Gene: MRAS & Disease: NS11, 18 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
635783	MRAS	c.212A>G	p.Gln71Arg (p.Q71R)	NM_001085049.3 M	SNV	P	1 +	4
635781	MRAS	c.68G>T	p.Gly23Val (p.G23V)	NM_001085049.3 M	SNV	P	2 +	4
635783	MRAS	c.212A>G	p.Gln71Arg (p.Q71R)	NM_001252090.2	SNV	P	1 +	4
	MRAS	c.-17A>G	--	NM_001252091.1	SNV	P	1 +	4
	MRAS	c.-17A>G	--	NM_001252092.2	SNV	P	1 +	4
	MRAS	c.-17A>G	--	NM_001252093.2	SNV	P	1 +	4
	MRAS	c.212A>G	p.Gln71Arg (p.Q71R)	NM_012219.4	SNV	P	1 +	4
635781	MRAS	c.68G>T	p.Gly23Val (p.G23V)	NM_012219.4	SNV	P	2 +	4
	MRAS	c.68G>T	p.Gly23Val (p.G23V)	NM_001252090.2	SNV	P	2 +	4
	MRAS	c.-35-24373G>T	--	NM_001252091.1	SNV	P	2 +	4
	MRAS	c.-36+24184G>T	--	NM_001252093.2	SNV	P	2 +	4
	MRAS	c.-36+23919G>T	--	NM_001252092.2	SNV	P	2 +	4
635782	MRAS	c.203C>T	p.Thr68Ile (p.T68I)	NM_001085049.3 M	SNV	P	1 +	2
	MRAS	c.203C>T	p.Thr68Ile (p.T68I)	NM_012219.4	SNV	P	1 +	2
	MRAS	c.203C>T	p.Thr68Ile (p.T68I)	NM_001252090.2	SNV	P	1 +	2
	MRAS	c.-26C>T	--	NM_001252091.1	SNV	P	1 +	2
	MRAS	c.-26C>T	--	NM_001252092.2	SNV	P	1 +	2
	MRAS	c.-26C>T	--	NM_001252093.2	SNV	P	1 +	2

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