CLDN23[gene] and "single gene"[properties] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2618954	NM_194284.3(CLDN23):c.32T>C (p.Met11Thr)	CLDN23 (M11T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558055	NM_194284.3(CLDN23):c.41C>T (p.Ala14Val)	CLDN23 (A14V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256412	NM_194284.3(CLDN23):c.63C>G (p.Asn21Lys)	CLDN23 (N21K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509064	NM_194284.3(CLDN23):c.98T>G (p.Val33Gly)	CLDN23 (V33G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145496	NM_194284.3(CLDN23):c.104G>A (p.Gly35Asp)	CLDN23 (G35D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145497	NM_194284.3(CLDN23):c.175C>T (p.Arg59Cys)	CLDN23 (R59C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594900	NM_194284.3(CLDN23):c.176G>A (p.Arg59His)	CLDN23 (R59H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658375	NM_194284.3(CLDN23):c.268G>A (p.Ala90Thr)	CLDN23 (A90T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2468907	NM_194284.3(CLDN23):c.329A>G (p.Asn110Ser)	CLDN23 (N110S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279197	NM_194284.3(CLDN23):c.334G>A (p.Val112Met)	CLDN23 (V112M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312879	NM_194284.3(CLDN23):c.382G>A (p.Gly128Ser)	CLDN23 (G128S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2320066	NM_194284.3(CLDN23):c.458C>T (p.Thr153Met)	CLDN23 (T153M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145499	NM_194284.3(CLDN23):c.460G>T (p.Val154Leu)	CLDN23 (V154L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381159	NM_194284.3(CLDN23):c.484C>G (p.Leu162Val)	CLDN23 (L162V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531890	NM_194284.3(CLDN23):c.511C>A (p.Leu171Met)	CLDN23 (L171M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259676	NM_194284.3(CLDN23):c.551G>C (p.Trp184Ser)	CLDN23 (W184S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336818	NM_194284.3(CLDN23):c.592G>A (p.Ala198Thr)	CLDN23 (A198T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616353	NM_194284.3(CLDN23):c.679G>A (p.Gly227Ser)	CLDN23 (G227S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522189	NM_194284.3(CLDN23):c.709C>A (p.Arg237Ser)	CLDN23 (R237S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215990	NM_194284.3(CLDN23):c.743C>G (p.Pro248Arg)	CLDN23 (P248R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145500	NM_194284.3(CLDN23):c.787G>A (p.Val263Ile)	CLDN23 (V263I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285642	NM_194284.3(CLDN23):c.793G>T (p.Asp265Tyr)	CLDN23 (D265Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 441783	GRCh37/hg19 8p23.1(chr8:8396736-8629734)x1	CLDN23	Copy number loss	See cases	GLikely benign

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Items: 23