"ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 377779	NM_006736.6(DNAJB2):c.195C>T (p.Tyr65=)	DNAJB2	Single nucleotide variant (synonymous variant)	Neuronopathy, distal hereditary motor, autosomal recessive 5 +3 more	GLikely benign
Select item 1330564	NM_006736.6(DNAJB2):c.233C>T (p.Thr78Ile)	DNAJB2 (T78I)	Single nucleotide variant (missense variant)	Neuronopathy, distal hereditary motor, autosomal recessive 5	GUncertain significance
Select item 917201	NM_006736.6(DNAJB2):c.446-17C>G	DNAJB2	Single nucleotide variant (intron variant)	Neuronopathy, distal hereditary motor, autosomal recessive 5 +1 more	GLikely benign
Select item 439620	NM_006736.6(DNAJB2):c.703C>G (p.Gln235Glu)	DNAJB2 (Q235E)	Single nucleotide variant (missense variant)	not specified +4 more	GLikely benign
Select item 289991	NM_006736.6(DNAJB2):c.808G>C (p.Gly270Arg)	DNAJB2 (G270R)	Single nucleotide variant (missense variant)	Neuronopathy, distal hereditary motor, autosomal recessive 5 +2 more	GBenign
Select item 2921162	NM_006736.6(DNAJB2):c.928C>T (p.Arg310Cys)	DNAJB2 (R310C)	Single nucleotide variant (missense variant +1 more)	Neuronopathy, distal hereditary motor, autosomal recessive 5	GUncertain significance

ClinVar