"Ambry Genetics"[submitter] AND "ZIC4"[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2207465	NM_032153.6(ZIC4):c.971C>A (p.Ala324Glu)	ZIC4 (A374E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306087	NM_032153.6(ZIC4):c.968C>G (p.Ala323Gly)	ZIC4 (A323G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522222	NM_032153.6(ZIC4):c.815A>G (p.Asp272Gly)	ZIC4 (D322G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2049047	NM_032153.6(ZIC4):c.794C>T (p.Thr265Met)	ZIC4 (T303M +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2616441	NM_032153.6(ZIC4):c.793A>C (p.Thr265Pro)	ZIC4 (T315P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623413	NM_032153.6(ZIC4):c.790T>C (p.Tyr264His)	ZIC4 (Y264H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548742	NM_032153.6(ZIC4):c.783C>G (p.Asp261Glu)	ZIC4 (D261E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193570	NM_032153.6(ZIC4):c.776C>G (p.Thr259Ser)	ZIC4 (T309S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331943	NM_032153.6(ZIC4):c.550C>G (p.Pro184Ala)	ZIC4 (P222A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2612168	NM_032153.6(ZIC4):c.529G>A (p.Glu177Lys)	ZIC4 (E227K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193569	NM_032153.6(ZIC4):c.427C>T (p.Leu143Phe)	ZIC4 (L181F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554223	NM_032153.6(ZIC4):c.351C>A (p.Phe117Leu)	ZIC4 (F117L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252026	NM_032153.6(ZIC4):c.326C>A (p.Ala109Glu)	ZIC4 (A109E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2173933	NM_032153.6(ZIC4):c.277G>T (p.Ala93Ser)	ZIC4 (A143S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2209026	NM_032153.6(ZIC4):c.236C>T (p.Pro79Leu)	ZIC4 (P117L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193568	NM_032153.6(ZIC4):c.235C>A (p.Pro79Thr)	ZIC4 (P117T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334709	NM_032153.6(ZIC4):c.188T>A (p.Leu63Gln)	ZIC4 (L113Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263765	NM_032153.6(ZIC4):c.182G>C (p.Gly61Ala)	ZIC4 (G111A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411693	NM_032153.6(ZIC4):c.149C>G (p.Pro50Arg)	ZIC4 (P50R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611042	NM_032153.6(ZIC4):c.140A>G (p.His47Arg)	ZIC4 (H47R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334708	NM_032153.6(ZIC4):c.136C>A (p.Leu46Ile)	ZIC4 (L46I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363642	NM_032153.6(ZIC4):c.127T>G (p.Phe43Val)	ZIC4 (F43V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350807	NM_032153.6(ZIC4):c.74G>A (p.Ser25Asn)	ZIC4 (S25N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2394328	NM_032153.6(ZIC4):c.50G>A (p.Arg17Gln)	ZIC4 (R55Q +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2208988	NM_032153.6(ZIC4):c.40C>T (p.Arg14Trp)	ZIC4 (R52W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238476	NM_032153.6(ZIC4):c.-7T>G	ZIC4 (S48R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2419216	NM_032153.6(ZIC4):c.-15-1225G>A	ZIC4 (R21K)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2396339	NM_032153.6(ZIC4):c.-16+986C>T	ZIC4 (S32F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334710	NM_032153.6(ZIC4):c.-16+967A>T	ZIC4 (R26W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329441	NM_032153.6(ZIC4):c.-16+952G>A	ZIC4 (A21T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2203866	NM_032153.6(ZIC4):c.-16+901C>T	ZIC4 (P4S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 31