"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "DNAJC13 - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 747153	NM_015268.4(DNAJC13):c.108T>C (p.Thr36=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 760600	NM_015268.4(DNAJC13):c.654T>C (p.Tyr218=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 780031	NM_015268.4(DNAJC13):c.932+15_932+16del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 767932	NM_015268.4(DNAJC13):c.932+16del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 767933	NM_015268.4(DNAJC13):c.1450-9dup	DNAJC13	Duplication (intron variant)	not provided	GBenign
Select item 774426	NM_015268.4(DNAJC13):c.2292-6G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 723361	NM_015268.4(DNAJC13):c.2336A>G (p.Lys779Arg)	DNAJC13 (K779R +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 773448	NM_015268.4(DNAJC13):c.2369C>A (p.Ser790Tyr)	DNAJC13 (S790Y +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 720116	NM_015268.4(DNAJC13):c.2517T>C (p.Asp839=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1026421	NM_015268.4(DNAJC13):c.2529A>C (p.Glu843Asp)	DNAJC13 (E843D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 724843	NM_015268.4(DNAJC13):c.2550-10T>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 733480	NM_015268.4(DNAJC13):c.2550-6del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 769279	NM_015268.4(DNAJC13):c.2736G>A (p.Arg912=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 728942	NM_015268.4(DNAJC13):c.2979+3A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 770706	NM_015268.4(DNAJC13):c.3594T>C (p.Thr1198=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 715477	NM_015268.4(DNAJC13):c.3872A>G (p.Glu1291Gly)	DNAJC13 (E1291G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 709668	NM_015268.4(DNAJC13):c.3942G>A (p.Pro1314=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 712441	NM_015268.4(DNAJC13):c.4305C>T (p.Leu1435=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 779231	NM_015268.4(DNAJC13):c.4385G>A (p.Arg1462His)	DNAJC13 (R1462H +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 785063	NM_015268.4(DNAJC13):c.4546C>T (p.Arg1516Cys)	DNAJC13 (R1516C +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 708389	NM_015268.4(DNAJC13):c.4813A>G (p.Ile1605Val)	DNAJC13 (I1610V +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 736836	NM_015268.4(DNAJC13):c.4999-8_4999-7del	DNAJC13	Deletion (intron variant)	not provided	GLikely benign
Select item 785064	NM_015268.4(DNAJC13):c.5385+7G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 725109	NM_015268.4(DNAJC13):c.5578C>T (p.Leu1860=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 709669	NM_015268.4(DNAJC13):c.5855A>C (p.Asn1952Thr)	DNAJC13 (N1952T +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 785866	NM_015268.4(DNAJC13):c.5886+10A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 739555	NM_015268.4(DNAJC13):c.5934T>G (p.Leu1978=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 726578	NM_015268.4(DNAJC13):c.5953T>C (p.Leu1985=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 778112	NM_015268.4(DNAJC13):c.5979C>T (p.Ala1993=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 719416	NM_015268.4(DNAJC13):c.5983G>C (p.Val1995Leu)	DNAJC13 (V2000L +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 734555	NM_015268.4(DNAJC13):c.6150T>G (p.His2050Gln)	DNAJC13 (H2050Q +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 735297	NM_015268.4(DNAJC13):c.6423C>T (p.Leu2141=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 778113	NM_015268.4(DNAJC13):c.6626-6T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 771354	NM_015268.4(DNAJC13):c.6675G>A (p.Met2225Ile)	DNAJC13 (M2225I +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1452099	NC_000003.11:g.(?_120365818)_(133465047_?)del	MBD4, MCM2 +109 more	Deletion	Alkaptonuria	GPathogenic
Select item 831681	NC_000003.12:g.(?_132465995)_(132722355_?)dup	ACAD11, ACKR4 +3 more	Duplication	Nephronophthisis	GUncertain significance

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Items: 36