"Ambry Genetics"[submitter] AND "MORC4"[gene] - ClinVar

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

Search results

Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3200179	NM_024657.5(MORC4):c.2596C>T (p.His866Tyr)	MORC4 (H866Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551909	NM_024657.5(MORC4):c.2593A>G (p.Thr865Ala)	MORC4 (T865A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200175	NM_024657.5(MORC4):c.2584G>A (p.Glu862Lys)	MORC4 (E862K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527289	NM_024657.5(MORC4):c.2465C>T (p.Ala822Val)	MORC4 (A822V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246077	NM_024657.5(MORC4):c.2298G>T (p.Gln766His)	MORC4 (Q766H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328653	NM_024657.5(MORC4):c.2233A>T (p.Ile745Phe)	MORC4 (I745F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495324	NM_024657.5(MORC4):c.2210C>T (p.Ser737Phe)	MORC4 (S737F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200161	NM_024657.5(MORC4):c.1958G>A (p.Arg653His)	MORC4 (R653H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2386839	NM_024657.5(MORC4):c.1830C>G (p.Asn610Lys)	MORC4 (N610K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200154	NM_024657.5(MORC4):c.1816C>A (p.Pro606Thr)	MORC4 (P606T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594443	NM_024657.5(MORC4):c.1756C>T (p.Pro586Ser)	MORC4 (P586S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366422	NM_024657.5(MORC4):c.1569G>C (p.Lys523Asn)	LOC121853063, MORC4 (K523N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212141	NM_024657.5(MORC4):c.1552G>A (p.Ala518Thr)	LOC121853063, MORC4 (A518T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411546	NM_024657.5(MORC4):c.1499A>G (p.Glu500Gly)	MORC4 (E500G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296114	NM_024657.5(MORC4):c.1252A>G (p.Ile418Val)	MORC4 (I418V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494866	NM_024657.5(MORC4):c.1207A>C (p.Lys403Gln)	MORC4 (K403Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599685	NM_024657.5(MORC4):c.1165A>G (p.Ile389Val)	MORC4 (I389V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383879	NM_024657.5(MORC4):c.1028C>T (p.Ser343Phe)	MORC4 (S343F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238580	NM_024657.5(MORC4):c.987G>C (p.Gln329His)	MORC4 (Q329H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200219	NM_024657.5(MORC4):c.973A>G (p.Lys325Glu)	MORC4 (K325E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301299	NM_024657.5(MORC4):c.920A>T (p.Tyr307Phe)	MORC4 (Y307F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200210	NM_024657.5(MORC4):c.911A>G (p.Tyr304Cys)	MORC4 (Y304C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286146	NM_024657.5(MORC4):c.716A>C (p.Gln239Pro)	MORC4 (Q239P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348969	NM_024657.5(MORC4):c.596G>A (p.Arg199His)	MORC4 (R199H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254767	NM_024657.5(MORC4):c.595C>T (p.Arg199Cys)	MORC4 (R199C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215092	NM_024657.5(MORC4):c.544G>A (p.Glu182Lys)	MORC4 (E182K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245132	NM_024657.5(MORC4):c.426T>G (p.Asn142Lys)	MORC4 (N142K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289928	NM_024657.5(MORC4):c.193G>A (p.Asp65Asn)	MORC4 (D65N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481310	NM_024657.5(MORC4):c.105G>T (p.Met35Ile)	MORC4 (M35I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594117	NM_024657.5(MORC4):c.53T>A (p.Leu18Gln)	MORC4 (L18Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226020	NM_024657.5(MORC4):c.46T>G (p.Cys16Gly)	MORC4 (C16G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200168	NM_024657.5(MORC4):c.19G>T (p.Ala7Ser)	MORC4 (A7S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250101	NM_024657.5(MORC4):c.11A>C (p.Tyr4Ser)	MORC4 (Y4S)	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: 33