Mutation Direct

Effortless mutation search and display tool

Search criteria：

Gene: NRAS & Disease: Rasopathy, 102 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
177778	NRAS	c.34G>A	p.Gly12Ser (p.G12S)	NM_002524.5 M	SNV	P	13 +	39
73058	NRAS	c.181C>A	p.Gln61Lys (p.Q61K)	NM_002524.5 M	SNV	P	24 +	39
39648	NRAS	c.35G>A	p.Gly12Asp (p.G12D)	NM_002524.5 M	SNV	P	14 +	34
40470	NRAS	c.35G>T	p.Gly12Val (p.G12V)	NM_002524.5 M	SNV	P	10 +	24
219097	NRAS	c.35G>C	p.Gly12Ala (p.G12A)	NM_002524.5 M	SNV	P	10 +	22
375874	NRAS	c.182A>T	p.Gln61Leu (p.Q61L)	NM_002524.5 M	SNV	P	21 +	19
13902	NRAS	c.149C>T	p.Thr50Ile (p.T50I)	NM_002524.5 M	SNV	P	4 +	17
1070042	NRAS	c.173C>T	p.Thr58Ile (p.T58I)	NM_002524.5 M	SNV	P	4 +	11
44575	NRAS	c.291-8G>A	--	NM_002524.5 M	SNV	LB	1 +	10
516515	NRAS	c.290+15A>C	--	NM_002524.5 M	SNV	LB	1 +	10
1582033	NRAS	c.273G>A	p.Ala91= (p.A91=)	NM_002524.5 M	SNV	LB	1 +	10
380330	NRAS	c.36T>G	p.Gly12= (p.G12=)	NM_002524.5 M	SNV	LB	2 +	9
561348	NRAS	c.112-24dup	--	NM_002524.5 M	Dup	LB	1 +	5
178104	NRAS	c.225C>T	p.Gly75= (p.G75=)	NM_002524.5 M	SNV	LB	2 +	5
418807	NRAS	c.451-21_451-19del	--	NM_002524.5 M	Del	LB	1 +	5
13903	NRAS	c.179G>A	p.Gly60Glu (p.G60E)	NM_002524.5 M	SNV	P	3 +	4
2189829	NRAS	c.450+6G>T	--	NM_002524.5 M	SNV	VUS	1 +	2
2059335	NRAS	c.290+4C>T	--	NM_002524.5 M	SNV	VUS	1 +	2
848828	NRAS	c.291-3T>C	--	NM_002524.5 M	SNV	VUS	1 +	2
2074072	NRAS	c.450G>C	p.Gln150His (p.Q150H)	NM_002524.5 M	SNV	VUS	1 +	2

102 Results, 20 per Page