DPF3[gene] and "single gene"[properties] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3085450	NM_001280542.3(DPF3):c.871+3078A>G	DPF3 (T405A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476614	NM_001280542.3(DPF3):c.871+3020G>C	DPF3 (E330D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361394	NM_001280542.3(DPF3):c.871+2959C>T	DPF3 (T320M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2246626	NM_001280542.3(DPF3):c.871+2937G>T	DPF3 (A303S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3085459	NM_001280542.3(DPF3):c.853G>A (p.Ala285Thr)	DPF3 (A285T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085458	NM_001280542.3(DPF3):c.829C>T (p.Arg277Trp)	DPF3 (R277W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623069	NM_001280542.3(DPF3):c.811A>T (p.Met271Leu)	DPF3 (M271L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085457	NM_001280542.3(DPF3):c.809A>G (p.Asn270Ser)	DPF3 (N280S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460759	NM_001280542.3(DPF3):c.755C>T (p.Pro252Leu)	DPF3 (P252L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273578	NM_001280542.3(DPF3):c.712C>T (p.Pro238Ser)	DPF3 (P238S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085456	NM_001280542.3(DPF3):c.677A>T (p.Glu226Val)	DPF3 (E236V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085455	NM_001280542.3(DPF3):c.589C>T (p.Pro197Ser)	DPF3 (P197S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085454	NM_001280542.3(DPF3):c.582C>A (p.His194Gln)	DPF3 (H204Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085453	NM_001280542.3(DPF3):c.532G>A (p.Gly178Ser)	DPF3 (G178S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464411	NM_001280542.3(DPF3):c.529C>T (p.Arg177Cys)	DPF3 (R232C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517590	NM_001280542.3(DPF3):c.523C>T (p.Arg175Trp)	DPF3 (R230W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284459	NM_001280542.3(DPF3):c.433G>A (p.Val145Ile)	DPF3 (V145I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393764	NM_001280542.3(DPF3):c.426A>G (p.Ile142Met)	DPF3 (I142M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273577	NM_001280542.3(DPF3):c.367C>T (p.Arg123Cys)	DPF3 (R133C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512140	NM_001280542.3(DPF3):c.271C>G (p.Pro91Ala)	DPF3 (P101A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403305	NM_001280542.3(DPF3):c.269A>T (p.Asp90Val)	DPF3 (D90V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1238152	NM_001280542.3(DPF3):c.253T>C (p.Leu85=)	DPF3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3085452	NM_001280542.3(DPF3):c.238C>T (p.Arg80Cys)	DPF3 (R90C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409550	NM_001280542.3(DPF3):c.154A>G (p.Asn52Asp)	DPF3 (N62D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085451	NM_001280542.3(DPF3):c.109G>A (p.Val37Met)	DPF3 (V92M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475226	NM_001280542.3(DPF3):c.76A>C (p.Ser26Arg)	DPF3 (S36R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319895	NM_001280542.3(DPF3):c.40G>A (p.Asp14Asn)	DPF3 (D14N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27