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Gene: KRAS & Disease: GASC, 54 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
12582	KRAS	c.35G>A	p.Gly12Asp (p.G12D)	NM_004985.5 M	SNV	P	14 +	52
	KRAS	c.35G>A	p.Gly12Asp (p.G12D)	NM_033360.4 MP	SNV	P	14 +	52
	KRAS	c.35G>A	p.Gly12Asp (p.G12D)	NM_001369786.1	SNV	P	14 +	52
	KRAS	c.35G>A	p.Gly12Asp (p.G12D)	NM_001369787.1	SNV	P	14 +	52
12584	KRAS	c.34G>A	p.Gly12Ser (p.G12S)	NM_004985.5 M	SNV	P	6 +	27
	KRAS	c.34G>A	p.Gly12Ser (p.G12S)	NM_033360.4 MP	SNV	P	6 +	27
	KRAS	c.34G>A	p.Gly12Ser (p.G12S)	NM_001369786.1	SNV	P	6 +	27
	KRAS	c.34G>A	p.Gly12Ser (p.G12S)	NM_001369787.1	SNV	P	6 +	27
40452	KRAS	c.65A>G	p.Gln22Arg (p.Q22R)	NM_004985.5 M	SNV	P	15 +	9
	KRAS	c.65A>G	p.Gln22Arg (p.Q22R)	NM_033360.4 MP	SNV	P	15 +	9
	KRAS	c.65A>G	p.Gln22Arg (p.Q22R)	NM_001369786.1	SNV	P	15 +	9
	KRAS	c.65A>G	p.Gln22Arg (p.Q22R)	NM_001369787.1	SNV	P	15 +	9
45119	KRAS	c.24A>G	p.Val8= (p.V8=)	NM_004985.5 M	SNV	LB	12 +	2
379556	KRAS	c.451-18A>G	--	NM_004985.5 M	SNV	LB	12 +	2
626130	KRAS	c.112-5C>T	--	NM_004985.5 M	SNV	LB	12 +	2
177714	KRAS	c.112-9C>T	--	NM_004985.5 M	SNV	LB	12 +	2
1046139	KRAS	c.388_389delinsAT	p.Ala130Ile (p.A130I)	NM_004985.5 M	Indel	VUS	12 +	2
180052	KRAS	c.451-5652C>T	--	NM_004985.5 M	SNV	LB	11 +	2
45119	KRAS	c.24A>G	p.Val8= (p.V8=)	NM_033360.4 MP	SNV	LB	12 +	2
379556	KRAS	c.5-18A>G	--	NM_033360.4 MP	SNV	LB	12 +	2

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