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

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

Search results

Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2569107	NM_007156.5(ZXDA):c.2362A>T (p.Asn788Tyr)	ZXDA (N788Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260189	NM_007156.5(ZXDA):c.2269G>A (p.Val757Ile)	ZXDA (V757I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469965	NM_007156.5(ZXDA):c.2267G>A (p.Ser756Asn)	ZXDA (S756N)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2346432	NM_007156.5(ZXDA):c.2251G>A (p.Ala751Thr)	ZXDA (A751T)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2346130	NM_007156.5(ZXDA):c.2194A>G (p.Thr732Ala)	ZXDA (T732A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3260190	NM_007156.5(ZXDA):c.2117A>G (p.Asp706Gly)	ZXDA (D706G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3199653	NM_007156.5(ZXDA):c.2044A>C (p.Thr682Pro)	ZXDA (T682P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225727	NM_007156.5(ZXDA):c.1748C>A (p.Ser583Tyr)	ZXDA (S583Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199652	NM_007156.5(ZXDA):c.1720C>A (p.Leu574Ile)	ZXDA (L574I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199650	NM_007156.5(ZXDA):c.1618A>C (p.Thr540Pro)	ZXDA (T540P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541717	NM_007156.5(ZXDA):c.1467A>C (p.Lys489Asn)	ZXDA (K489N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199649	NM_007156.5(ZXDA):c.1211G>A (p.Ser404Asn)	ZXDA (S404N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199648	NM_007156.5(ZXDA):c.1138C>A (p.Arg380Ser)	ZXDA (R380S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199647	NM_007156.5(ZXDA):c.1136A>T (p.Gln379Leu)	ZXDA (Q379L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320307	NM_007156.5(ZXDA):c.1100A>G (p.Glu367Gly)	ZXDA (E367G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199656	NM_007156.5(ZXDA):c.823G>A (p.Gly275Arg)	ZXDA (G275R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199655	NM_007156.5(ZXDA):c.813G>C (p.Glu271Asp)	ZXDA (E271D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539946	NM_007156.5(ZXDA):c.758G>A (p.Gly253Asp)	LOC130068358, ZXDA (G253D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473159	NM_007156.5(ZXDA):c.748G>T (p.Ala250Ser)	LOC130068358, ZXDA (A250S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388825	NM_007156.5(ZXDA):c.743T>C (p.Leu248Pro)	LOC130068358, ZXDA (L248P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2262317	NM_007156.5(ZXDA):c.736G>A (p.Glu246Lys)	LOC130068358, ZXDA (E246K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494311	NM_007156.5(ZXDA):c.710C>T (p.Pro237Leu)	LOC130068358, ZXDA (P237L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369411	NM_007156.5(ZXDA):c.624A>C (p.Gln208His)	LOC130068358, ZXDA (Q208H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284136	NM_007156.5(ZXDA):c.617C>T (p.Ala206Val)	LOC130068358, ZXDA (A206V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260191	NM_007156.5(ZXDA):c.535G>A (p.Gly179Ser)	ZXDA (G179S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328530	NM_007156.5(ZXDA):c.535G>C (p.Gly179Arg)	ZXDA (G179R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242818	NM_007156.5(ZXDA):c.526T>C (p.Phe176Leu)	ZXDA (F176L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400978	NM_007156.5(ZXDA):c.487G>A (p.Gly163Ser)	ZXDA (G163S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536127	NM_007156.5(ZXDA):c.475G>C (p.Ala159Pro)	ZXDA (A159P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495559	NM_007156.5(ZXDA):c.413A>G (p.Gln138Arg)	ZXDA (Q138R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377029	NM_007156.5(ZXDA):c.388G>A (p.Ala130Thr)	ZXDA (A130T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357197	NM_007156.5(ZXDA):c.377A>G (p.Asp126Gly)	ZXDA (D126G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2349199	NM_007156.5(ZXDA):c.356C>A (p.Ala119Glu)	ZXDA (A119E)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3199654	NM_007156.5(ZXDA):c.298G>T (p.Val100Leu)	ZXDA (V100L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396458	NM_007156.5(ZXDA):c.261C>A (p.Asp87Glu)	ZXDA (D87E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199651	NM_007156.5(ZXDA):c.166G>A (p.Gly56Arg)	ZXDA (G56R)	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: 36