Favorite

Mutation Direct

Effortless mutation search and display tool

Search criteria：

Gene: FLCN & Disease: Familial Spontaneous Pneumothorax, 921 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
3363	FLCN	c.1285dupC	--	NM_144997.7 M	Dup	P	6 +	27
	FLCN	c.1285dup	p.His429fs (p.H429fs)	NM_144997.7 M	Dup	P	6 +	27
	FLCN	c.1339dup	p.His447fs (p.H447fs)	NM_001353229.2	Dup	P	6 +	27
	FLCN	c.1285dup	p.His429fs (p.H429fs)	NM_001353230.2	Dup	P	6 +	27
	FLCN	c.1285dup	p.His429fs (p.H429fs)	NM_001353231.2	Dup	P	6 +	27
186785	FLCN	c.466TTC[1]	p.Phe157Del (p.F157del)	NM_144997.7 M	MS	P	6 +	13
186785	FLCN	c.469_471del	--	NM_144997.7 M	MS	P	6 +	13
3364	FLCN	c.1285delC	--	NM_144997.7 M	Del	P	6 +	13
3364	FLCN	c.1285del	p.His429fs (p.H429fs)	NM_144997.7 M	Del	P	6 +	13
186785	FLCN	c.520TTC[1]	p.Phe175Del (p.F175del)	NM_001353229.2	MS	P	6 +	13
	FLCN	c.466TTC[1]	p.Phe157Del (p.F157del)	NM_001353230.2	MS	P	6 +	13
	FLCN	c.466TTC[1]	p.Phe157Del (p.F157del)	NM_001353231.2	MS	P	6 +	13
	FLCN	c.466TTC[1]	p.Phe157Del (p.F157del)	NM_144606.7	MS	P	6 +	13
3364	FLCN	c.1339del	p.His447fs (p.H447fs)	NM_001353229.2	Del	P	6 +	13
	FLCN	c.1285del	p.His429fs (p.H429fs)	NM_001353230.2	Del	P	6 +	13
	FLCN	c.1285del	p.His429fs (p.H429fs)	NM_001353231.2	Del	P	6 +	13
253251	FLCN	c.1429C>T	p.Arg477Ter (p.R477X)	NM_144997.7 M	SNV	P	6 +	12
	FLCN	c.1483C>T	p.Arg495Ter (p.R495X)	NM_001353229.2	SNV	P	6 +	12
	FLCN	c.1429C>T	p.Arg477Ter (p.R477X)	NM_001353230.2	SNV	P	6 +	12
	FLCN	c.1429C>T	p.Arg477Ter (p.R477X)	NM_001353231.2	SNV	P	6 +	12

921 Results, 20 per Page

...

Comparison