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Mutation Direct

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Gene: SOS2 & Disease: NS9, 1084 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
986082	SOS2	c.1648C>G	p.Arg550Gly (p.R550G)	NM_006939.4 M	SNV	LP	1 +	8
577079	SOS2	c.800T>G	p.Met267Arg (p.M267R)	NM_006939.4 M	SNV	P	4 +	7
542404	SOS2	c.2854G>A	p.Asp952Asn (p.D952N)	NM_006939.4 M	SNV	LB	2 +	4
475762	SOS2	c.816T>C	p.Ser272= (p.S272=)	NM_006939.4 M	SNV	B	2 +	3
684626	SOS2	c.791C>A	p.Thr264Lys (p.T264K)	NM_006939.4 M	SNV	P	4 +	3
384710	SOS2	c.2232C>T	p.Asn744= (p.N744=)	NM_006939.4 M	SNV	B	1 +	3
384711	SOS2	c.3813G>A	p.Pro1271= (p.P1271=)	NM_006939.4 M	SNV	B	1 +	3
376857	SOS2	c.3235A>G	p.Thr1079Ala (p.T1079A)	NM_006939.4 M	SNV	LB	1 +	2
1605815	SOS2	c.3984A>G	p.Ala1328= (p.A1328=)	NM_006939.4 M	SNV	LB	1 +	2
1507530	SOS2	c.1747A>G	p.Asn583Asp (p.N583D)	NM_006939.4 M	SNV	VUS	1 +	2
917721	SOS2	c.813C>T	p.Ser271= (p.S271=)	NM_006939.4 M	SNV	LB	1 +	2
811274	SOS2	c.2712A>G	p.Glu904= (p.E904=)	NM_006939.4 M	SNV	LB	1 +	2
704803	SOS2	c.1767C>T	p.Asn589= (p.N589=)	NM_006939.4 M	SNV	LB	1 +	2
377127	SOS2	c.2317G>C	p.Asp773His (p.D773H)	NM_006939.4 M	SNV	LB	3 +	2
2146622	SOS2	c.345+5C>T	--	NM_006939.4 M	SNV	VUS	1 +	2
1098117	SOS2	c.3360A>C	p.Pro1120= (p.P1120=)	NM_006939.4 M	SNV	LB	1 +	2
1515954	SOS2	c.1197-3T>C	--	NM_006939.4 M	SNV	VUS	1 +	2
705054	SOS2	c.399A>C	p.Val133= (p.V133=)	NM_006939.4 M	SNV	LB	2 +	2
705089	SOS2	c.195G>A	p.Arg65= (p.R65=)	NM_006939.4 M	SNV	LB	1 +	2
639562	SOS2	c.2366T>C	p.Leu789Ser (p.L789S)	NM_006939.4 M	SNV	LB	1 +	2

1084 Results, 20 per Page

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