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Mutation Direct

Effortless mutation search and display tool

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Gene: EXOSC9 & Disease: Cerebral Atrophy, 2 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
549845	EXOSC9	c.41T>C	p.Leu14Pro (p.L14P)	NM_005033.3 M	SNV	P	2 +	4
549845	EXOSC9	c.41T>C	p.Leu14Pro (p.L14P)	NM_001034194.2	SNV	P	2 +	4

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