"Ambry Genetics"[submitter] AND "NIN"[gene] - ClinVar - NCBI

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

Search results

Items: 1 to 100 of 140

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2254604	NM_020921.4(NIN):c.6289A>G (p.Lys2097Glu)	NIN (K2097E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363574	NM_020921.4(NIN):c.6206C>G (p.Thr2069Ser)	NIN (T2069S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349559	NM_020921.4(NIN):c.6156G>C (p.Arg2052Ser)	NIN (R1339S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325657	NM_020921.4(NIN):c.6155G>C (p.Arg2052Thr)	NIN (R2052T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2155125	NM_020921.4(NIN):c.6154A>G (p.Arg2052Gly)	NIN (R1339G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2608288	NM_020921.4(NIN):c.6138A>T (p.Lys2046Asn)	NIN (K2046N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200093	NM_020921.4(NIN):c.6097G>T (p.Val2033Leu)	NIN (V1320L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243943	NM_020921.4(NIN):c.6030C>A (p.His2010Gln)	NIN (H2010Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200092	NM_020921.4(NIN):c.5988G>C (p.Gln1996His)	NIN (Q1283H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604511	NM_020921.4(NIN):c.5968C>T (p.Pro1990Ser)	NIN (P1277S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361104	NM_020921.4(NIN):c.5960C>T (p.Pro1987Leu)	NIN (P1274L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200091	NM_020921.4(NIN):c.5957G>A (p.Cys1986Tyr)	NIN (C1986Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200090	NM_020921.4(NIN):c.5945A>T (p.Gln1982Leu)	NIN (Q1982L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299754	NM_020921.4(NIN):c.5920C>G (p.His1974Asp)	NIN (H1974D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617237	NM_020921.4(NIN):c.5863G>A (p.Glu1955Lys)	NIN (E1242K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1916111	NM_020921.4(NIN):c.5733G>C (p.Glu1911Asp)	NIN (E1198D +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3200089	NM_020921.4(NIN):c.5732A>G (p.Glu1911Gly)	NIN (E1911G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321333	NM_020921.4(NIN):c.5710G>A (p.Glu1904Lys)	NIN (E1191K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533475	NM_020921.4(NIN):c.5692A>G (p.Met1898Val)	NIN (M1898V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3299750	NM_020921.4(NIN):c.5670A>C (p.Lys1890Asn)	NIN (K1177N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2177570	NM_020921.4(NIN):c.5633G>A (p.Arg1878His)	NIN (R1165H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1899384	NM_020921.4(NIN):c.5620C>T (p.Arg1874Trp)	NIN (R1161W +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2225147	NM_020921.4(NIN):c.5586G>A (p.Met1862Ile)	NIN (M1862I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468373	NM_020921.4(NIN):c.5533A>C (p.Met1845Leu)	NIN (M1845L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296715	NM_020921.4(NIN):c.5520G>C (p.Lys1840Asn)	NIN (K1840N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2053939	NM_020921.4(NIN):c.5483G>C (p.Gly1828Ala)	NIN (G1828A +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2069883	NM_020921.4(NIN):c.5473C>T (p.His1825Tyr)	NIN (H1112Y +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2599039	NM_020921.4(NIN):c.5438C>G (p.Ala1813Gly)	NIN (A1100G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3200088	NM_020921.4(NIN):c.5413T>C (p.Ser1805Pro)	NIN (S1805P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200087	NM_020921.4(NIN):c.5390A>C (p.Glu1797Ala)	NIN (E1797A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2196067	NM_020921.4(NIN):c.5351G>A (p.Arg1784Gln)	NIN (R1071Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2280953	NM_020921.4(NIN):c.5330A>G (p.Asn1777Ser)	NIN (N1064S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1898845	NM_020921.4(NIN):c.5323G>C (p.Val1775Leu)	NIN (V1062L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2554766	NM_020921.4(NIN):c.5263G>A (p.Ala1755Thr)	NIN (A1042T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2985209	NM_020921.4(NIN):c.5222C>T (p.Ala1741Val)	NIN (A1028V +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3200086	NM_020921.4(NIN):c.5182G>A (p.Asp1728Asn)	LOC126861936, NIN (D1015N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200085	NM_020921.4(NIN):c.4984C>A (p.Leu1662Ile)	NIN (L1662I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299753	NM_020921.4(NIN):c.4936C>T (p.Arg1646Cys)	NIN (R933C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299554	NM_020921.4(NIN):c.4900G>A (p.Glu1634Lys)	NIN (E1634K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1336157	NM_020921.4(NIN):c.4898G>A (p.Arg1633Gln)	NIN (R1633Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3200084	NM_020921.4(NIN):c.4867A>G (p.Lys1623Glu)	NIN (K1623E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2183463	NM_020921.4(NIN):c.4853T>G (p.Leu1618Arg)	NIN (L1618R +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2064763	NM_020921.4(NIN):c.4838G>A (p.Arg1613His)	NIN (R1613H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2391681	NM_020921.4(NIN):c.4697C>G (p.Ala1566Gly)	NIN (A853G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611071	NM_020921.4(NIN):c.4652A>G (p.Gln1551Arg)	NIN (Q838R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312073	NM_020921.4(NIN):c.4628A>T (p.Lys1543Ile)	NIN (K1543I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380009	NM_020921.4(NIN):c.4564G>C (p.Glu1522Gln)	NIN (E1522Q +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3299743	NM_020921.4(NIN):c.4459A>G (p.Lys1487Glu)	NIN (K1487E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1991727	NM_020921.4(NIN):c.4418C>T (p.Thr1473Ile)	NIN (T1473I)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2327234	NM_020921.4(NIN):c.4410G>C (p.Glu1470Asp)	NIN (E1470D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400800	NM_020921.4(NIN):c.4381T>G (p.Leu1461Val)	NIN (L1461V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2491059	NM_020921.4(NIN):c.4198C>G (p.Leu1400Val)	NIN (L1400V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299745	NM_020921.4(NIN):c.4151T>C (p.Ile1384Thr)	NIN (I1384T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238137	NM_020921.4(NIN):c.4096C>T (p.Leu1366Phe)	NIN (L1366F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2812428	NM_020921.4(NIN):c.4059G>C (p.Glu1353Asp)	NIN (E1353D)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2085074	NM_020921.4(NIN):c.3988G>A (p.Gly1330Ser)	NIN (G1330S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2476718	NM_020921.4(NIN):c.3770G>A (p.Arg1257Gln)	NIN (R1257Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 435998	NM_020921.4(NIN):c.3749T>C (p.Leu1250Pro)	NIN (L1250P)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2391658	NM_020921.4(NIN):c.3742T>C (p.Tyr1248His)	NIN (Y1248H)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2618279	NM_020921.4(NIN):c.3736C>G (p.Pro1246Ala)	NIN (P1246A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2029654	NM_020921.4(NIN):c.3727G>C (p.Glu1243Gln)	NIN (E1243Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3001803	NM_020921.4(NIN):c.3721A>C (p.Ile1241Leu)	NIN (I1241L)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 211610	NM_020921.4(NIN):c.3647G>A (p.Arg1216Gln)	NIN (R1216Q)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2163811	NM_020921.4(NIN):c.3611A>G (p.Gln1204Arg)	NIN (Q1204R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2599482	NM_020921.4(NIN):c.3535G>A (p.Gly1179Ser)	NIN (G1179S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2517474	NM_020921.4(NIN):c.3509T>C (p.Ile1170Thr)	NIN (I1170T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471398	NM_020921.4(NIN):c.3499G>A (p.Glu1167Lys)	NIN (E1167K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239362	NM_020921.4(NIN):c.3425A>T (p.His1142Leu)	NIN (H1142L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1940498	NM_020921.4(NIN):c.3424C>T (p.His1142Tyr)	NIN (H1142Y)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2334988	NM_020921.4(NIN):c.3407A>G (p.Glu1136Gly)	NIN (E1136G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1336725	NM_020921.4(NIN):c.3403G>A (p.Val1135Ile)	NIN (V1135I)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2403506	NM_020921.4(NIN):c.3395C>T (p.Thr1132Met)	NIN (T1132M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 1912467	NM_020921.4(NIN):c.3388A>C (p.Asn1130His)	NIN (N1130H)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3299749	NM_020921.4(NIN):c.3364C>G (p.Gln1122Glu)	NIN (Q1122E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299747	NM_020921.4(NIN):c.3356C>G (p.Thr1119Ser)	NIN (T1119S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3200081	NM_020921.4(NIN):c.3298C>T (p.Pro1100Ser)	NIN (P1100S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200080	NM_020921.4(NIN):c.3287A>G (p.Gln1096Arg)	NIN (Q1096R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2887332	NM_020921.4(NIN):c.3269G>C (p.Arg1090Thr)	NIN (R1090T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3299744	NM_020921.4(NIN):c.3128A>T (p.Glu1043Val)	NIN (E1043V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2078804	NM_020921.4(NIN):c.3097C>A (p.Gln1033Lys)	NIN (Q1033K)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2537385	NM_020921.4(NIN):c.3019G>A (p.Glu1007Lys)	NIN (E1007K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 211605	NM_020921.4(NIN):c.3007C>G (p.Arg1003Gly)	NIN (R1003G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226171	NM_020921.4(NIN):c.2858A>T (p.Glu953Val)	NIN (E953V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3200079	NM_020921.4(NIN):c.2741A>T (p.Gln914Leu)	NIN (Q914L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2040615	NM_020921.4(NIN):c.2704A>G (p.Lys902Glu)	NIN (K902E)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2889370	NM_020921.4(NIN):c.2668C>G (p.Leu890Val)	NIN (L890V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2561762	NM_020921.4(NIN):c.2657C>A (p.Thr886Asn)	NIN (T886N)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2617118	NM_020921.4(NIN):c.2647G>A (p.Glu883Lys)	NIN (E883K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2178476	NM_020921.4(NIN):c.2609C>T (p.Ala870Val)	NIN (A870V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3200078	NM_020921.4(NIN):c.2526A>T (p.Gln842His)	NIN (Q842H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526482	NM_020921.4(NIN):c.2495C>G (p.Ala832Gly)	NIN (A832G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508981	NM_020921.4(NIN):c.2425A>G (p.Arg809Gly)	NIN (R809G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354226	NM_020921.4(NIN):c.2238G>C (p.Gln746His)	NIN (Q746H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2533163	NM_020921.4(NIN):c.2083T>A (p.Cys695Ser)	NIN (C695S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308760	NM_020921.4(NIN):c.2026A>G (p.Ile676Val)	LOC130055602, NIN (I676V)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2379891	NM_020921.4(NIN):c.2024A>T (p.Glu675Val)	LOC130055602, NIN (E675V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2237282	NM_020921.4(NIN):c.1999A>G (p.Lys667Glu)	LOC130055602, NIN (K667E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 436001	NM_020921.4(NIN):c.1991C>T (p.Thr664Ile)	LOC130055602, NIN (T664I)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2295344	NM_020921.4(NIN):c.1987C>T (p.His663Tyr)	LOC130055602, NIN (H663Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299748	NM_020921.4(NIN):c.1933G>A (p.Val645Ile)	LOC130055602, NIN (V645I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 2