MOV10[gene] and "single gene"[properties] - ClinVar

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Items: 50

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 783293	NM_001321324.2(MOV10):c.78G>A (p.Leu26=)	MOV10	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3200727	NM_001321324.2(MOV10):c.83T>G (p.Met28Arg)	MOV10 (M28R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221440	NM_001321324.2(MOV10):c.94C>A (p.Arg32Ser)	MOV10 (R32S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2568814	NM_001321324.2(MOV10):c.235C>G (p.Leu79Val)	MOV10 (L23V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318919	NM_001321324.2(MOV10):c.236T>C (p.Leu79Pro)	MOV10 (L23P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470998	NM_001321324.2(MOV10):c.284T>C (p.Leu95Pro)	MOV10 (L39P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457611	NM_001321324.2(MOV10):c.327G>T (p.Lys109Asn)	MOV10 (K109N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295270	NM_001321324.2(MOV10):c.368G>A (p.Gly123Asp)	MOV10 (G67D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3036675	NM_001321324.2(MOV10):c.418C>G (p.Leu140Val)	MOV10 (L140V +1 more)	Single nucleotide variant (missense variant)	MOV10-related disorder	GLikely benign
Select item 2603504	NM_001321324.2(MOV10):c.425G>A (p.Arg142His)	MOV10 (R142H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200712	NM_001321324.2(MOV10):c.467G>A (p.Arg156Gln)	MOV10 (R100Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713189	NM_001321324.2(MOV10):c.537C>T (p.Phe179=)	MOV10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2545623	NM_001321324.2(MOV10):c.597T>A (p.His199Gln)	MOV10 (H143Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518376	NM_001321324.2(MOV10):c.700A>C (p.Ile234Leu)	MOV10 (I234L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248607	NM_001321324.2(MOV10):c.703G>A (p.Ala235Thr)	MOV10 (A235T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 731932	NM_001321324.2(MOV10):c.774G>A (p.Arg258=)	MOV10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1342312	NM_001321324.2(MOV10):c.869C>T (p.Ala290Val)	MOV10 (A234V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2280505	NM_001321324.2(MOV10):c.961G>T (p.Ala321Ser)	MOV10 (A265S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593270	NM_001321324.2(MOV10):c.1085C>T (p.Ser362Leu)	MOV10 (S362L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 773150	NM_001321324.2(MOV10):c.1141-6C>T	MOV10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2287791	NM_001321324.2(MOV10):c.1240A>G (p.Lys414Glu)	MOV10 (K414E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468161	NM_001321324.2(MOV10):c.1396C>T (p.Arg466Cys)	MOV10 (R466C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200629	NM_001321324.2(MOV10):c.1433C>T (p.Pro478Leu)	MOV10 (P478L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200634	NM_001321324.2(MOV10):c.1441G>A (p.Val481Ile)	MOV10 (V481I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3200637	NM_001321324.2(MOV10):c.1473G>A (p.Lys491=)	MOV10	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2392069	NM_001321324.2(MOV10):c.1703G>A (p.Arg568Gln)	MOV10 (R568Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 770115	NM_001321324.2(MOV10):c.1779+5T>C	MOV10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2321997	NM_001321324.2(MOV10):c.1792T>G (p.Trp598Gly)	MOV10 (W598G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 731063	NM_001321324.2(MOV10):c.1797C>T (p.Asp599=)	MOV10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2603684	NM_001321324.2(MOV10):c.1798G>A (p.Ala600Thr)	MOV10 (A544T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780257	NM_001321324.2(MOV10):c.1893G>C (p.Ser631=)	MOV10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3200646	NM_001321324.2(MOV10):c.1958C>G (p.Pro653Arg)	MOV10 (P597R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200650	NM_001321324.2(MOV10):c.2123C>T (p.Thr708Ile)	MOV10 (T652I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602853	NM_001321324.2(MOV10):c.2138A>T (p.Tyr713Phe)	MOV10 (Y713F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548885	NM_001321324.2(MOV10):c.2147G>A (p.Gly716Asp)	MOV10 (G660D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513328	NM_001321324.2(MOV10):c.2272G>A (p.Val758Met)	MOV10 (V702M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604185	NM_001321324.2(MOV10):c.2285G>A (p.Arg762His)	MOV10 (R706H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786401	NM_001321324.2(MOV10):c.2294G>A (p.Arg765His)	MOV10 (R765H +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2599011	NM_001321324.2(MOV10):c.2300C>T (p.Ala767Val)	MOV10 (A767V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200676	NM_001321324.2(MOV10):c.2360G>A (p.Arg787His)	MOV10 (R731H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200682	NM_001321324.2(MOV10):c.2462G>A (p.Arg821His)	MOV10 (R765H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467824	NM_001321324.2(MOV10):c.2521C>T (p.Arg841Cys)	MOV10 (R785C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481311	NM_001321324.2(MOV10):c.2689G>A (p.Gly897Ser)	MOV10 (G897S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 929739	NM_001321324.2(MOV10):c.2831A>G (p.Tyr944Cys)	MOV10 (Y888C +1 more)	Single nucleotide variant (missense variant)	Premature ovarian failure	GUncertain significance
Select item 2553993	NM_001321324.2(MOV10):c.2942T>A (p.Leu981His)	MOV10 (L981H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200694	NM_001321324.2(MOV10):c.2947C>G (p.Gln983Glu)	MOV10 (Q983E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200697	NM_001321324.2(MOV10):c.2954G>A (p.Arg985Gln)	MOV10 (R929Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2623609	NM_001321324.2(MOV10):c.2969G>T (p.Gly990Val)	MOV10 (G934V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 711972	NM_001321324.2(MOV10):c.2979G>T (p.Leu993=)	MOV10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2331069	NM_001321324.2(MOV10):c.2997G>C (p.Trp999Cys)	MOV10 (W943C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 50