"PreventionGenetics, part of Exact Sciences"[submitter] AND "DNAJC3"[g - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 710813	NM_006260.5(DNAJC3):c.78C>T (p.Tyr26=)	DNAJC3	Single nucleotide variant (synonymous variant)	DNAJC3-related disorder +1 more	GBenign
Select item 3050286	NM_006260.5(DNAJC3):c.111T>A (p.Val37=)	DNAJC3	Single nucleotide variant (synonymous variant)	DNAJC3-related disorder	GLikely benign
Select item 724566	NM_006260.5(DNAJC3):c.162T>G (p.Ala54=)	DNAJC3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 735587	NM_006260.5(DNAJC3):c.297A>G (p.Gln99=)	DNAJC3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3045640	NM_006260.5(DNAJC3):c.729-3C>T	DNAJC3	Single nucleotide variant (intron variant)	DNAJC3-related disorder	GLikely benign
Select item 768623	NM_006260.5(DNAJC3):c.848+10T>C	DNAJC3	Single nucleotide variant (intron variant)	DNAJC3-related disorder +1 more	GBenign
Select item 717316	NM_006260.5(DNAJC3):c.1060G>C (p.Glu354Gln)	DNAJC3 (E354Q)	Single nucleotide variant (missense variant)	DNAJC3-related disorder +2 more	GBenign/Likely benign
Select item 3051786	NM_006260.5(DNAJC3):c.1323T>A (p.Asp441Glu)	DNAJC3 (D441E)	Single nucleotide variant (missense variant)	DNAJC3-related disorder	GLikely benign
Select item 3050332	NM_006260.5(DNAJC3):c.1398T>C (p.Asp466=)	DNAJC3	Single nucleotide variant (synonymous variant)	DNAJC3-related disorder	GLikely benign