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Gene: WDR37 & Disease: NOCGUS, 16 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
633618	WDR37	c.389C>T	p.Thr130Ile (p.T130I)	NM_014023.4 M	SNV	P	5 +	4
440948	WDR37	c.374C>T	p.Thr125Ile (p.T125I)	NM_014023.4 M	SNV	P	6 +	4
633616	WDR37	c.386C>G	p.Ser129Cys (p.S129C)	NM_014023.4 M	SNV	P	5 +	3
633617	WDR37	c.356C>T	p.Ser119Phe (p.S119F)	NM_014023.4 M	SNV	P	5 +	3
1185321	WDR37	c.726+22T>C	--	NM_014023.4 M	SNV	B	1 +	1
1279921	WDR37	c.659A>G	p.Asp220Gly (p.D220G)	NM_014023.4 M	SNV	LP	1 +	1
1279922	WDR37	c.778G>A	p.Asp260Asn (p.D260N)	NM_014023.4 M	SNV	LP	1 +	1
1279923	WDR37	c.770C>A	p.Pro257His (p.P257H)	NM_014023.4 M	SNV	VUS	1 +	1
1699001	WDR37	c.850G>T	p.Val284Phe (p.V284F)	NM_014023.4 M	SNV	VUS	1 +	1
1031227	WDR37	c.344C>T	p.Thr115Ile (p.T115I)	NM_014023.4 M	SNV	P	1 +	1
1683656	WDR37	c.928G>A	p.Val310Met (p.V310M)	NM_014023.4 M	SNV	VUS	1 +	1
1175763	WDR37	c.406A>T	p.Ser136Cys (p.S136C)	NM_014023.4 M	SNV	LP	1 +	1
2441964	WDR37	c.808A>C	p.Ile270Leu (p.I270L)	NM_014023.4 M	SNV	VUS	1 +	1
2506456	WDR37	c.727-27_727-24del	--	NM_014023.4 M	MS	LP	1 +	1
1341782	WDR37	c.808A>G	p.Ile270Val (p.I270V)	NM_014023.4 M	SNV	VUS	1 +	0
1342458	WDR37	c.1444G>C	p.Gly482Arg (p.G482R)	NM_014023.4 M	SNV	VUS	1 +	0

16 Results, 20 per Page

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