"Ambry Genetics"[submitter] AND "DNAJC9"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2491551	NM_173348.2(FAM149B1):c.1184G>A (p.Arg395Gln)	DNAJC9, FAM149B1 (R395Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091893	NM_173348.2(FAM149B1):c.1188T>G (p.Asn396Lys)	DNAJC9, FAM149B1 (N396K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091895	NM_173348.2(FAM149B1):c.1199G>A (p.Arg400Gln)	DNAJC9, FAM149B1 (R400Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286578	NM_173348.2(FAM149B1):c.1212T>G (p.Phe404Leu)	DNAJC9, FAM149B1 (F404L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2371495	NM_173348.2(FAM149B1):c.1237G>A (p.Val413Met)	DNAJC9, FAM149B1 (V413M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388178	NM_173348.2(FAM149B1):c.1255C>T (p.Arg419Cys)	DNAJC9, FAM149B1 (R419C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091896	NM_173348.2(FAM149B1):c.1273A>G (p.Thr425Ala)	DNAJC9, FAM149B1 (T425A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091897	NM_173348.2(FAM149B1):c.1343G>A (p.Gly448Glu)	DNAJC9, FAM149B1 (G448E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374141	NM_173348.2(FAM149B1):c.1345G>C (p.Ala449Pro)	DNAJC9, FAM149B1 (A449P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325965	NM_173348.2(FAM149B1):c.1345G>A (p.Ala449Thr)	DNAJC9, FAM149B1 (A449T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360865	NM_173348.2(FAM149B1):c.1349G>A (p.Arg450Gln)	DNAJC9, FAM149B1 (R450Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455465	NM_173348.2(FAM149B1):c.1391C>A (p.Thr464Lys)	DNAJC9, FAM149B1 (T464K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277191	NM_173348.2(FAM149B1):c.1489G>A (p.Asp497Asn)	DNAJC9, FAM149B1 (D497N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360673	NM_173348.2(FAM149B1):c.1516G>A (p.Val506Met)	DNAJC9, FAM149B1 (V506M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238986	NM_173348.2(FAM149B1):c.1589C>G (p.Thr530Ser)	DNAJC9, FAM149B1 (T530S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367861	NM_173348.2(FAM149B1):c.1618C>T (p.Arg540Cys)	DNAJC9, FAM149B1 (R540C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530170	NM_173348.2(FAM149B1):c.1631C>T (p.Ala544Val)	DNAJC9, FAM149B1 (A544V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339601	NM_173348.2(FAM149B1):c.1643C>T (p.Pro548Leu)	DNAJC9, FAM149B1 (P548L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484414	NM_173348.2(FAM149B1):c.1648C>A (p.Gln550Lys)	DNAJC9, FAM149B1 (Q550K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361458	NM_015190.5(DNAJC9):c.692T>C (p.Met231Thr)	DNAJC9, FAM149B1 (M231T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244756	NM_015190.5(DNAJC9):c.633A>C (p.Glu211Asp)	DNAJC9, FAM149B1 (E211D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609661	NM_015190.5(DNAJC9):c.394C>G (p.Gln132Glu)	DNAJC9 (Q132E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304998	NM_015190.5(DNAJC9):c.389T>C (p.Ile130Thr)	DNAJC9 (I130T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318040	NM_015190.5(DNAJC9):c.362A>G (p.Lys121Arg)	DNAJC9 (K121R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322848	NM_015190.5(DNAJC9):c.221A>T (p.Gln74Leu)	DNAJC9, LOC126860955 (Q74L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261977	NM_015190.5(DNAJC9):c.203T>C (p.Val68Ala)	DNAJC9, LOC126860955 (V68A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273139	NM_015190.5(DNAJC9):c.71G>T (p.Arg24Leu)	DNAJC9, LOC126860955 (R24L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27