"Ambry Genetics"[submitter] AND "MOV10L1"[gene] - ClinVar

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Items: 78

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2277045	NM_018995.3(MOV10L1):c.19A>G (p.Lys7Glu)	MOV10L1 (K7E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340410	NM_018995.3(MOV10L1):c.85G>C (p.Glu29Gln)	MOV10L1 (E29Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368159	NM_018995.3(MOV10L1):c.118G>A (p.Val40Ile)	MOV10L1 (V20I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240247	NM_018995.3(MOV10L1):c.118G>C (p.Val40Leu)	MOV10L1 (V20L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200779	NM_018995.3(MOV10L1):c.170T>C (p.Met57Thr)	MOV10L1 (M37T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281391	NM_018995.3(MOV10L1):c.223C>A (p.Gln75Lys)	MOV10L1 (Q55K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526342	NM_018995.3(MOV10L1):c.224A>G (p.Gln75Arg)	MOV10L1 (Q55R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332718	NM_018995.3(MOV10L1):c.233T>C (p.Ile78Thr)	MOV10L1 (I58T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483392	NM_018995.3(MOV10L1):c.239T>C (p.Val80Ala)	MOV10L1 (V60A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200887	NM_018995.3(MOV10L1):c.299A>G (p.Asp100Gly)	MOV10L1 (D80G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206462	NM_018995.3(MOV10L1):c.313G>A (p.Asp105Asn)	MOV10L1 (D85N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615801	NM_018995.3(MOV10L1):c.422C>G (p.Ser141Cys)	MOV10L1 (S121C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200930	NM_018995.3(MOV10L1):c.439G>A (p.Glu147Lys)	MOV10L1 (E147K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200935	NM_018995.3(MOV10L1):c.443G>C (p.Gly148Ala)	MOV10L1 (G128A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200938	NM_018995.3(MOV10L1):c.487A>T (p.Ile163Phe)	MOV10L1 (I143F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200943	NM_018995.3(MOV10L1):c.490C>T (p.Arg164Trp)	MOV10L1 (R164W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200946	NM_018995.3(MOV10L1):c.510C>G (p.Ser170Arg)	MOV10L1 (S170R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376456	NM_018995.3(MOV10L1):c.511G>A (p.Glu171Lys)	MOV10L1 (E171K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403379	NM_018995.3(MOV10L1):c.653G>A (p.Arg218Gln)	MOV10L1 (R218Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462132	NM_018995.3(MOV10L1):c.779A>G (p.Tyr260Cys)	MOV10L1 (Y240C +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2263520	NM_018995.3(MOV10L1):c.830C>T (p.Thr277Met)	MOV10L1 (T257M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200962	NM_018995.3(MOV10L1):c.854G>A (p.Gly285Glu)	MOV10L1 (G285E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200970	NM_018995.3(MOV10L1):c.973A>G (p.Lys325Glu)	MOV10L1 (K305E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511900	NM_018995.3(MOV10L1):c.991G>A (p.Val331Met)	MOV10L1 (V311M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481586	NM_018995.3(MOV10L1):c.1028C>T (p.Ser343Leu)	MOV10L1 (S343L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357527	NM_018995.3(MOV10L1):c.1094G>A (p.Ser365Asn)	MOV10L1 (S345N +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2517782	NM_018995.3(MOV10L1):c.1108A>G (p.Asn370Asp)	MOV10L1 (N350D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348128	NM_018995.3(MOV10L1):c.1229A>G (p.Lys410Arg)	MOV10L1 (K410R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351996	NM_018995.3(MOV10L1):c.1232C>A (p.Thr411Asn)	MOV10L1 (T391N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517055	NM_018995.3(MOV10L1):c.1409C>T (p.Ala470Val)	MOV10L1 (A450V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251643	NM_018995.3(MOV10L1):c.1499T>G (p.Ile500Ser)	MOV10L1 (I480S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251644	NM_018995.3(MOV10L1):c.1604C>T (p.Ser535Leu)	MOV10L1 (S515L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210821	NM_018995.3(MOV10L1):c.1661T>C (p.Met554Thr)	MOV10L1 (M534T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513567	NM_018995.3(MOV10L1):c.1673T>C (p.Ile558Thr)	MOV10L1 (I538T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2462197	NM_018995.3(MOV10L1):c.1721C>T (p.Ala574Val)	MOV10L1 (A554V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407648	NM_018995.3(MOV10L1):c.1738C>G (p.Leu580Val)	MOV10L1 (L560V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464267	NM_018995.3(MOV10L1):c.1744G>A (p.Ala582Thr)	MOV10L1 (A562T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3200790	NM_018995.3(MOV10L1):c.1753A>C (p.Lys585Gln)	MOV10L1 (K565Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200795	NM_018995.3(MOV10L1):c.1781A>G (p.Asn594Ser)	MOV10L1 (N574S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200798	NM_018995.3(MOV10L1):c.1834G>A (p.Val612Ile)	MOV10L1 (V592I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244682	NM_018995.3(MOV10L1):c.1835T>C (p.Val612Ala)	MOV10L1 (V612A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383872	NM_018995.3(MOV10L1):c.1885A>G (p.Met629Val)	MOV10L1 (M609V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621923	NM_018995.3(MOV10L1):c.1951A>T (p.Ile651Phe)	MOV10L1 (I631F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200813	NM_018995.3(MOV10L1):c.2011A>G (p.Thr671Ala)	MOV10L1 (T671A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228163	NM_018995.3(MOV10L1):c.2099A>T (p.Glu700Val)	MOV10L1 (E680V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519562	NM_018995.3(MOV10L1):c.2140C>T (p.Pro714Ser)	MOV10L1 (P694S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234341	NM_018995.3(MOV10L1):c.2152C>A (p.Pro718Thr)	MOV10L1 (P718T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549044	NM_018995.3(MOV10L1):c.2297A>G (p.Tyr766Cys)	MOV10L1 (Y746C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355289	NM_018995.3(MOV10L1):c.2384G>A (p.Arg795Gln)	MOV10L1 (R775Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200835	NM_018995.3(MOV10L1):c.2477G>A (p.Arg826Gln)	MOV10L1 (R806Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291575	NM_018995.3(MOV10L1):c.2500G>A (p.Glu834Lys)	MOV10L1 (E814K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200840	NM_018995.3(MOV10L1):c.2521G>A (p.Val841Ile)	MOV10L1 (V821I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2295576	NM_018995.3(MOV10L1):c.2538A>C (p.Arg846Ser)	MOV10L1 (R846S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200845	NM_018995.3(MOV10L1):c.2566C>T (p.Arg856Cys)	MOV10L1 (R836C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594540	NM_018995.3(MOV10L1):c.2567G>A (p.Arg856His)	MOV10L1 (R836H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396405	NM_018995.3(MOV10L1):c.2572C>T (p.Arg858Trp)	MOV10L1 (R858W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277384	NM_018995.3(MOV10L1):c.2666G>A (p.Gly889Glu)	MOV10L1 (G869E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546556	NM_018995.3(MOV10L1):c.2731G>A (p.Val911Met)	MOV10L1 (V891M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269492	NM_018995.3(MOV10L1):c.2750T>C (p.Met917Thr)	MOV10L1 (M897T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382457	NM_018995.3(MOV10L1):c.2782G>T (p.Ala928Ser)	MOV10L1 (A55S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525595	NM_018995.3(MOV10L1):c.2792A>G (p.Tyr931Cys)	MOV10L1 (Y58C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216071	NM_018995.3(MOV10L1):c.2824A>G (p.Met942Val)	MOV10L1 (M922V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556626	NM_018995.3(MOV10L1):c.2831G>A (p.Arg944Gln)	MOV10L1 (R924Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350821	NM_018995.3(MOV10L1):c.2853A>C (p.Glu951Asp)	MOV10L1 (E78D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241848	NM_018995.3(MOV10L1):c.2885C>T (p.Pro962Leu)	MOV10L1 (P89L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479255	NM_018995.3(MOV10L1):c.2930C>T (p.Ala977Val)	MOV10L1 (A104V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200884	NM_018995.3(MOV10L1):c.2990C>G (p.Pro997Arg)	MOV10L1 (P997R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559092	NM_018995.3(MOV10L1):c.2996T>C (p.Val999Ala)	MOV10L1 (V126A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621718	NM_018995.3(MOV10L1):c.3065G>A (p.Arg1022Gln)	MOV10L1 (R1002Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249888	NM_018995.3(MOV10L1):c.3242G>A (p.Arg1081His)	MOV10L1 (R1061H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200893	NM_018995.3(MOV10L1):c.3328C>T (p.Arg1110Trp)	MOV10L1 (R1110W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548351	NM_018995.3(MOV10L1):c.3398A>C (p.Asn1133Thr)	MOV10L1 (N1113T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200902	NM_018995.3(MOV10L1):c.3461G>A (p.Arg1154Gln)	MOV10L1 (R1154Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237899	NM_018995.3(MOV10L1):c.3500C>G (p.Thr1167Arg)	MOV10L1 (T1167R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200913	NM_018995.3(MOV10L1):c.3523G>A (p.Asp1175Asn)	MOV10L1 (D1175N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2212299	NM_018995.3(MOV10L1):c.3542A>G (p.Gln1181Arg)	MOV10L1 (Q1135R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313247	NM_018995.3(MOV10L1):c.3544T>C (p.Ser1182Pro)	MOV10L1 (S1182P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276437	NM_018995.3(MOV10L1):c.3548T>G (p.Leu1183Arg)	MOV10L1 (L310R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 78