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Gene: FGFR2 & Disease: GASC, 640 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
13272	FGFR2	c.755C>G	p.Ser252Trp (p.S252W)	NM_000141.5 M	SNV	P	17 +	33
	FGFR2	c.755C>G	p.Ser252Trp (p.S252W)	NM_022970.4 MP	SNV	P	17 +	33
	FGFR2	c.755C>G	p.Ser252Trp (p.S252W)	NM_001144913.1	SNV	P	17 +	33
	FGFR2	c.488C>G	p.Ser163Trp (p.S163W)	NM_001144915.2	SNV	P	17 +	33
	FGFR2	c.410C>G	p.Ser137Trp (p.S137W)	NM_001144916.2	SNV	P	17 +	33
	FGFR2	c.755C>G	p.Ser252Trp (p.S252W)	NM_001144917.2	SNV	P	17 +	33
	FGFR2	c.410C>G	p.Ser137Trp (p.S137W)	NM_001144918.2	SNV	P	17 +	33
	FGFR2	c.488C>G	p.Ser163Trp (p.S163W)	NM_001144919.2	SNV	P	17 +	33
	FGFR2	c.71C>G	p.Ser24Trp (p.S24W)	NM_001320654.2	SNV	P	17 +	33
	FGFR2	c.755C>G	p.Ser252Trp (p.S252W)	NM_001320658.2	SNV	P	17 +	33
	FGFR2	c.488C>G	p.Ser163Trp (p.S163W)	NM_023029.2	SNV	P	17 +	33
	FGFR2	c.749-4844C>G	--	NM_001144914.1	SNV	P	17 +	33
13273	FGFR2	c.758C>G	p.Pro253Arg (p.P253R)	NM_000141.5 M	SNV	P	14 +	15
	FGFR2	c.758C>G	p.Pro253Arg (p.P253R)	NM_022970.4 MP	SNV	P	14 +	15
	FGFR2	c.758C>G	p.Pro253Arg (p.P253R)	NM_001144913.1	SNV	P	14 +	15
	FGFR2	c.491C>G	p.Pro164Arg (p.P164R)	NM_001144915.2	SNV	P	14 +	15
	FGFR2	c.413C>G	p.Pro138Arg (p.P138R)	NM_001144916.2	SNV	P	14 +	15
	FGFR2	c.758C>G	p.Pro253Arg (p.P253R)	NM_001144917.2	SNV	P	14 +	15
	FGFR2	c.413C>G	p.Pro138Arg (p.P138R)	NM_001144918.2	SNV	P	14 +	15
	FGFR2	c.491C>G	p.Pro164Arg (p.P164R)	NM_001144919.2	SNV	P	14 +	15

640 Results, 20 per Page

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