DEPDC7[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2296365	NM_001077242.2(DEPDC7):c.37C>T (p.Leu13Phe)	DEPDC7 (L13F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081756	NM_001077242.2(DEPDC7):c.64A>G (p.Arg22Gly)	DEPDC7 (R22G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327212	NM_001077242.2(DEPDC7):c.80G>A (p.Ser27Asn)	DEPDC7 (S18N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377868	NM_001077242.2(DEPDC7):c.106A>G (p.Thr36Ala)	DEPDC7 (T36A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081753	NM_001077242.2(DEPDC7):c.319G>A (p.Val107Ile)	DEPDC7 (V98I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315162	NM_001077242.2(DEPDC7):c.466T>A (p.Tyr156Asn)	DEPDC7 (Y156N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081755	NM_001077242.2(DEPDC7):c.596T>C (p.Ile199Thr)	DEPDC7 (I190T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 992807	NM_001077242.2(DEPDC7):c.763A>T (p.Lys255Ter)	DEPDC7 (K246* +1 more)	Single nucleotide variant (nonsense)	Autism	GUncertain significance
Select item 2336157	NM_001077242.2(DEPDC7):c.865C>G (p.Pro289Ala)	DEPDC7 (P280A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376389	NM_001077242.2(DEPDC7):c.943C>T (p.Pro315Ser)	DEPDC7 (P306S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353967	NM_001077242.2(DEPDC7):c.1102G>A (p.Ala368Thr)	DEPDC7 (A368T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713409	NM_001077242.2(DEPDC7):c.1332T>G (p.Asn444Lys)	DEPDC7 (N435K +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2493302	NM_001077242.2(DEPDC7):c.1450A>G (p.Lys484Glu)	DEPDC7 (K484E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081752	NM_001077242.2(DEPDC7):c.1479G>T (p.Leu493Phe)	DEPDC7 (L484F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance