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Gene: KRAS & Disease: ECCL, 24 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
12580	KRAS	c.38G>A	p.Gly13Asp (p.G13D)	NM_004985.5 M	SNV	P	11 +	39
	KRAS	c.38G>A	p.Gly13Asp (p.G13D)	NM_033360.4 MP	SNV	P	11 +	39
	KRAS	c.38G>A	p.Gly13Asp (p.G13D)	NM_001369786.1	SNV	P	11 +	39
	KRAS	c.38G>A	p.Gly13Asp (p.G13D)	NM_001369787.1	SNV	P	11 +	39
197243	KRAS	c.436G>A	p.Ala146Thr (p.A146T)	NM_004985.5 M	SNV	P	4 +	18
	KRAS	c.436G>A	p.Ala146Thr (p.A146T)	NM_033360.4 MP	SNV	P	4 +	18
	KRAS	c.436G>A	p.Ala146Thr (p.A146T)	NM_001369786.1	SNV	P	4 +	18
	KRAS	c.436G>A	p.Ala146Thr (p.A146T)	NM_001369787.1	SNV	P	4 +	18
375962	KRAS	c.437C>T	p.Ala146Val (p.A146V)	NM_004985.5 M	SNV	P	6 +	16
	KRAS	c.437C>T	p.Ala146Val (p.A146V)	NM_033360.4 MP	SNV	P	6 +	16
	KRAS	c.437C>T	p.Ala146Val (p.A146V)	NM_001369786.1	SNV	P	6 +	16
	KRAS	c.437C>T	p.Ala146Val (p.A146V)	NM_001369787.1	SNV	P	6 +	16
375965	KRAS	c.351A>C	p.Lys117Asn (p.K117N)	NM_004985.5 M	SNV	P	7 +	10
	KRAS	c.351A>C	p.Lys117Asn (p.K117N)	NM_033360.4 MP	SNV	P	7 +	10
	KRAS	c.351A>C	p.Lys117Asn (p.K117N)	NM_001369786.1	SNV	P	7 +	10
	KRAS	c.351A>C	p.Lys117Asn (p.K117N)	NM_001369787.1	SNV	P	7 +	10

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