ZNF383[gene] and "single gene"[properties] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3195446	NM_001387601.1(ZNF383):c.35C>T (p.Ser12Phe)	ZNF383 (S12F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315255	NM_001387601.1(ZNF383):c.242C>T (p.Ser81Leu)	ZNF383 (S81L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335612	NM_001387601.1(ZNF383):c.261A>C (p.Leu87Phe)	ZNF383 (L87F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616803	NM_001387601.1(ZNF383):c.266C>T (p.Ser89Phe)	ZNF383 (S89F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2681666	NM_001387601.1(ZNF383):c.272A>T (p.Lys91Met)	ZNF383 (K91M)	Single nucleotide variant (missense variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 3335611	NM_001387601.1(ZNF383):c.307G>C (p.Glu103Gln)	ZNF383 (E103Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358428	NM_001387601.1(ZNF383):c.346A>G (p.Ser116Gly)	ZNF383 (S116G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598884	NM_001387601.1(ZNF383):c.566A>G (p.Gln189Arg)	ZNF383 (Q189R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331578	NM_001387601.1(ZNF383):c.601A>G (p.Lys201Glu)	ZNF383 (K201E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215804	NM_001387601.1(ZNF383):c.643C>T (p.Arg215Trp)	ZNF383 (R215W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402651	NM_001387601.1(ZNF383):c.758C>T (p.Pro253Leu)	ZNF383 (P253L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608637	NM_001387601.1(ZNF383):c.809T>C (p.Ile270Thr)	ZNF383 (I270T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240482	NM_001387601.1(ZNF383):c.853A>G (p.Lys285Glu)	ZNF383 (K285E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195447	NM_001387601.1(ZNF383):c.935G>A (p.Cys312Tyr)	ZNF383 (C312Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554632	NM_001387601.1(ZNF383):c.1010C>G (p.Pro337Arg)	ZNF383 (P337R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195443	NM_001387601.1(ZNF383):c.1061C>A (p.Thr354Asn)	ZNF383 (T354N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195444	NM_001387601.1(ZNF383):c.1110A>T (p.Glu370Asp)	ZNF383 (E370D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372215	NM_001387601.1(ZNF383):c.1171G>A (p.Glu391Lys)	ZNF383 (E391K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400957	NM_001387601.1(ZNF383):c.1264T>A (p.Tyr422Asn)	ZNF383 (Y422N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619020	NM_001387601.1(ZNF383):c.1333A>G (p.Thr445Ala)	ZNF383 (T445A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544363	NM_001387601.1(ZNF383):c.1399C>T (p.Arg467Cys)	ZNF383 (R467C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 21