Favorite

Mutation Direct

Effortless mutation search and display tool

Search criteria：

Gene: IL17F & Disease: CANDF6, 107 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
911491	IL17F	c.254+1G>A	--	NM_052872.4 M	SNV	B	1 +	2
1378990	IL17F	c.33+5G>A	--	NM_052872.4 M	SNV	VUS	1 +	2
30589	IL17F	c.284C>T	p.Ser95Leu (p.S95L)	NM_052872.4 M	SNV	P	1 +	2
225391	IL17F	c.254+1G>T	--	NM_052872.4 M	SNV	LB	1 +	1
2155639	IL17F	c.39G>A	p.Lys13= (p.K13=)	NM_052872.4 M	SNV	LB	1 +	1
660654	IL17F	c.391C>T	p.Arg131Trp (p.R131W)	NM_052872.4 M	SNV	VUS	1 +	1
1500904	IL17F	c.274C>T	p.Arg92Trp (p.R92W)	NM_052872.4 M	SNV	VUS	1 +	1
569602	IL17F	c.388G>A	p.Val130Ile (p.V130I)	NM_052872.4 M	SNV	VUS	1 +	1
1412057	IL17F	c.3G>C	p.Met1Ile (p.M1I)	NM_052872.4 M	SNV	VUS	1 +	1
1148961	IL17F	c.58T>C	p.Leu20= (p.L20=)	NM_052872.4 M	SNV	LB	1 +	0
539172	IL17F	c.177T>C	p.Ile59= (p.I59=)	NM_052872.4 M	SNV	LB	1 +	0
539173	IL17F	c.413_414del	p.Ser138fs (p.S138fs)	NM_052872.4 M	MS	LB	1 +	0
1488432	IL17F	c.53C>A	p.Ser18Ter (p.S18X)	NM_052872.4 M	SNV	VUS	1 +	0
2010679	IL17F	c.182T>A	p.Ile61Asn (p.I61N)	NM_052872.4 M	SNV	VUS	1 +	0
958519	IL17F	c.56T>C	p.Ile19Thr (p.I19T)	NM_052872.4 M	SNV	VUS	1 +	0
1641534	IL17F	c.180C>A	p.Gly60= (p.G60=)	NM_052872.4 M	SNV	LB	1 +	0
1037376	IL17F	c.388G>T	p.Val130Phe (p.V130F)	NM_052872.4 M	SNV	VUS	1 +	0
1361986	IL17F	c.214C>T	p.Arg72Cys (p.R72C)	NM_052872.4 M	SNV	VUS	1 +	0
964683	IL17F	c.352A>C	p.Met118Leu (p.M118L)	NM_052872.4 M	SNV	VUS	1 +	0
357463	IL17F	c.*243T>G	--	NM_052872.4 M	SNV	B	1 +	0

107 Results, 20 per Page

Comparison