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Mutation Direct

Effortless mutation search and display tool

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Gene: LMX1B & Disease: Nephrotic Syndrome, 3 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
498798	LMX1B	c.737G>A	p.Arg246Gln (p.R246Q)	NM_001174147.2 M	SNV	P	3 +	8
	LMX1B	c.737G>A	p.Arg246Gln (p.R246Q)	NM_001174146.2	SNV	P	3 +	8
	LMX1B	c.737G>A	p.Arg246Gln (p.R246Q)	NM_002316.4	SNV	P	3 +	8

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