ZNF382[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2396548	NM_032825.5(ZNF382):c.75C>A (p.Asp25Glu)	ZNF382 (D24E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532817	NM_032825.5(ZNF382):c.163A>G (p.Met55Val)	ZNF382 (M54V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301220	NM_032825.5(ZNF382):c.164T>G (p.Met55Arg)	ZNF382 (M55R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465240	NM_032825.5(ZNF382):c.170G>A (p.Arg57His)	ZNF382 (R57H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319889	NM_032825.5(ZNF382):c.214C>G (p.Pro72Ala)	ZNF382 (P72A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195438	NM_032825.5(ZNF382):c.238G>T (p.Asp80Tyr)	ZNF382 (D80Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264209	NM_032825.5(ZNF382):c.254A>G (p.Asp85Gly)	ZNF382 (D84G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228891	NM_032825.5(ZNF382):c.336G>C (p.Glu112Asp)	ZNF382 (E111D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195439	NM_032825.5(ZNF382):c.487G>A (p.Asp163Asn)	ZNF382 (D162N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335608	NM_032825.5(ZNF382):c.532A>G (p.Lys178Glu)	ZNF382 (K177E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483705	NM_032825.5(ZNF382):c.663C>G (p.Phe221Leu)	ZNF382 (F221L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195440	NM_032825.5(ZNF382):c.737G>A (p.Gly246Glu)	ZNF382 (G245E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335610	NM_032825.5(ZNF382):c.746T>G (p.Phe249Cys)	ZNF382 (F248C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217706	NM_032825.5(ZNF382):c.785T>C (p.Leu262Pro)	ZNF382 (L262P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195441	NM_032825.5(ZNF382):c.851T>C (p.Ile284Thr)	ZNF382 (I284T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319652	NM_032825.5(ZNF382):c.860A>C (p.Gln287Pro)	ZNF382 (Q286P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366924	NM_032825.5(ZNF382):c.934A>G (p.Ile312Val)	ZNF382 (I311V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270014	NM_032825.5(ZNF382):c.1084C>T (p.Arg362Cys)	ZNF382 (R361C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310057	NM_032825.5(ZNF382):c.1329G>T (p.Lys443Asn)	ZNF382 (K443N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463583	NM_032825.5(ZNF382):c.1420C>T (p.Arg474Cys)	ZNF382 (R473C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195435	NM_032825.5(ZNF382):c.1421G>A (p.Arg474His)	ZNF382 (R474H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542571	NM_032825.5(ZNF382):c.1475A>G (p.Asn492Ser)	ZNF382 (N491S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257035	NM_032825.5(ZNF382):c.1483C>G (p.Pro495Ala)	ZNF382 (P495A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335609	NM_032825.5(ZNF382):c.1484C>T (p.Pro495Leu)	ZNF382 (P494L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195436	NM_032825.5(ZNF382):c.1508G>A (p.Arg503Lys)	ZNF382 (R502K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281081	NM_032825.5(ZNF382):c.1600A>G (p.Asn534Asp)	ZNF382 (N533D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195437	NM_032825.5(ZNF382):c.1610T>C (p.Val537Ala)	ZNF382 (V536A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553393	NM_032825.5(ZNF382):c.1643G>A (p.Gly548Glu)	ZNF382 (G548E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 28