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Mutation Direct

Effortless mutation search and display tool

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Gene: WNT9B & Disease: CYSRD, 2 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
1344866	WNT9B	c.949G>A	p.Gly317Arg (p.G317R)	NM_003396.3 M	SNV	LP	2 +	1
1344866	WNT9B	c.904+45G>A	--	NM_001320458.2	SNV	LP	2 +	1

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