Gene Mutation Browser

Coriell Institute for Medical Research

Gene Mutations

Records Return: (5)

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Gene	Gene Omim Number	Disease Omim Number	Chromosome Location	Gene Mutation	Allelic Variant	Omim Phenotype	Sample Count
VCP	601023	167320	9p13-p12	ARG155CYS	0002	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA	8
VCP	601023	167320	9p13-p12	ARG155HIS	0001	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA	35
VCP	601023	167320	9p13-p12	ARG155PRO		INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA	1
VCP	601023	167320	9p13-p12	ARG159CYS		INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA	5
VCP	601023	167320	9p13-p12	LEU198TRP		INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA	7

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