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Mutation Direct

Effortless mutation search and display tool

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Gene: GPR179 & Disease: Congenital Stationary Night Blindness, 3 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
31204	GPR179	c.984del	p.Ser329fs (p.S329fs)	NM_001004334.4 M	Del	P	3 +	2
505393	GPR179	c.2706_2707dup	p.Pro903fs (p.P903fs)	NM_001004334.4 M	Dup	LP	1 +	2
286815	GPR179	c.799_803delinsTGATCTAC	p.Gln267_Val268delinsTer	NM_001004334.4 M	Indel	P	1 +	1

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