FAM186A[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	ACAD10, ACADS +4836 more	Copy number gain	See cases	GPathogenic
Select item 153751	GRCh38/hg38 12q13.12-13.13(chr12:50122359-53248460)x1	LOC130007898, LOC130007899 +206 more	Copy number loss	See cases	GPathogenic
Select item 2642979	NM_001145475.3(FAM186A):c.*8A>G	FAM186A	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 2607016	NM_001145475.3(FAM186A):c.6980T>G (p.Leu2327Arg)	FAM186A (L2327R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092179	NM_001145475.3(FAM186A):c.6952G>T (p.Gly2318Cys)	FAM186A (G2318C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478729	NM_001145475.3(FAM186A):c.6862C>A (p.Gln2288Lys)	FAM186A (Q2288K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283681	NM_001145475.3(FAM186A):c.6827C>T (p.Ser2276Phe)	FAM186A (S2276F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279494	NM_001145475.3(FAM186A):c.6779T>C (p.Phe2260Ser)	FAM186A (F2260S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277312	NM_001145475.3(FAM186A):c.6761T>C (p.Ile2254Thr)	FAM186A (I2254T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092178	NM_001145475.3(FAM186A):c.6691A>C (p.Asn2231His)	FAM186A (N2231H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092177	NM_001145475.3(FAM186A):c.6663G>T (p.Gln2221His)	FAM186A (Q2221H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092176	NM_001145475.3(FAM186A):c.6608A>G (p.Lys2203Arg)	FAM186A (K2203R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370559	NM_001145475.3(FAM186A):c.6601G>A (p.Gly2201Arg)	FAM186A (G2201R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1236725	NM_001145475.3(FAM186A):c.6579G>A (p.Met2193Ile)	FAM186A (M2193I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2624332	NM_001145475.3(FAM186A):c.6490A>T (p.Ile2164Phe)	FAM186A (I2164F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092175	NM_001145475.3(FAM186A):c.6475A>G (p.Ile2159Val)	FAM186A (I2159V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593852	NM_001145475.3(FAM186A):c.6397C>T (p.His2133Tyr)	FAM186A (H2133Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601337	NM_001145475.3(FAM186A):c.6379G>A (p.Gly2127Arg)	FAM186A (G2127R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213329	NM_001145475.3(FAM186A):c.6363G>C (p.Gln2121His)	FAM186A (Q2121H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289721	NM_001145475.3(FAM186A):c.6309G>T (p.Lys2103Asn)	FAM186A (K2103N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603343	NM_001145475.3(FAM186A):c.6280C>A (p.Pro2094Thr)	FAM186A (P2094T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557681	NM_001145475.3(FAM186A):c.6263C>T (p.Pro2088Leu)	FAM186A (P2088L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205714	NM_001145475.3(FAM186A):c.6206G>A (p.Arg2069Gln)	FAM186A (R2069Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3277305	NM_001145475.3(FAM186A):c.6170C>T (p.Ser2057Leu)	FAM186A (S2057L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513276	NM_001145475.3(FAM186A):c.6149T>C (p.Leu2050Pro)	FAM186A (L2050P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204074	NM_001145475.3(FAM186A):c.6148C>G (p.Leu2050Val)	FAM186A (L2050V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219036	NM_001145475.3(FAM186A):c.6127C>A (p.Pro2043Thr)	FAM186A (P2043T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601503	NM_001145475.3(FAM186A):c.5992G>A (p.Glu1998Lys)	FAM186A (E1998K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277314	NM_001145475.3(FAM186A):c.5942T>A (p.Val1981Asp)	FAM186A (V1981D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322646	NM_001145475.3(FAM186A):c.5935G>A (p.Ala1979Thr)	FAM186A (A1979T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385007	NM_001145475.3(FAM186A):c.5912C>T (p.Pro1971Leu)	FAM186A (P1971L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284927	NM_001145475.3(FAM186A):c.5879C>G (p.Ser1960Cys)	FAM186A (S1960C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277315	NM_001145475.3(FAM186A):c.5839T>C (p.Trp1947Arg)	FAM186A (W1947R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598094	NM_001145475.3(FAM186A):c.5755G>A (p.Ala1919Thr)	FAM186A (A1919T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481560	NM_001145475.3(FAM186A):c.5737T>C (p.Trp1913Arg)	FAM186A (W1913R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092171	NM_001145475.3(FAM186A):c.5699T>G (p.Leu1900Arg)	FAM186A (L1900R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379165	NM_001145475.3(FAM186A):c.5569T>G (p.Ser1857Ala)	FAM186A (S1857A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271421	NM_001145475.3(FAM186A):c.5503G>C (p.Gly1835Arg)	FAM186A (G1835R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277310	NM_001145475.3(FAM186A):c.5497A>G (p.Thr1833Ala)	FAM186A (T1833A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613905	NM_001145475.3(FAM186A):c.5486G>A (p.Arg1829Gln)	FAM186A (R1829Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350871	NM_001145475.3(FAM186A):c.5473C>T (p.Leu1825Phe)	FAM186A (L1825F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092170	NM_001145475.3(FAM186A):c.5462C>G (p.Ser1821Cys)	FAM186A (S1821C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407184	NM_001145475.3(FAM186A):c.5441C>T (p.Pro1814Leu)	FAM186A (P1814L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2619873	NM_001145475.3(FAM186A):c.5425A>G (p.Thr1809Ala)	FAM186A (T1809A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208316	NM_001145475.3(FAM186A):c.5387G>C (p.Arg1796Pro)	FAM186A (R1796P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2401196	NM_001145475.3(FAM186A):c.5386C>T (p.Arg1796Cys)	FAM186A (R1796C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277302	NM_001145475.3(FAM186A):c.5372C>A (p.Ala1791Glu)	FAM186A (A1791E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277309	NM_001145475.3(FAM186A):c.5369G>A (p.Gly1790Glu)	FAM186A (G1790E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461307	NM_001145475.3(FAM186A):c.5293G>C (p.Val1765Leu)	FAM186A (V1765L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213827	NM_001145475.3(FAM186A):c.5221G>A (p.Ala1741Thr)	FAM186A (A1741T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092169	NM_001145475.3(FAM186A):c.5093C>T (p.Thr1698Ile)	FAM186A (T1698I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307592	NM_001145475.3(FAM186A):c.5039C>T (p.Ala1680Val)	FAM186A (A1680V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374161	NM_001145475.3(FAM186A):c.4936G>A (p.Ala1646Thr)	FAM186A (A1646T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379016	NM_001145475.3(FAM186A):c.4895C>T (p.Ala1632Val)	FAM186A (A1632V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3025413	NM_001145475.3(FAM186A):c.4872G>T (p.Gly1624=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3024807	NM_001145475.3(FAM186A):c.4866T>C (p.Ala1622=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2672503	NM_001145475.3(FAM186A):c.4860C>G (p.Ala1620=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2468428	NM_001145475.3(FAM186A):c.4835G>C (p.Gly1612Ala)	FAM186A (G1612A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234410	NM_001145475.3(FAM186A):c.4823C>T (p.Ala1608Val)	FAM186A (A1608V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372705	NM_001145475.3(FAM186A):c.4822G>A (p.Ala1608Thr)	FAM186A (A1608T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2672504	NM_001145475.3(FAM186A):c.4800G>T (p.Gly1600=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3092168	NM_001145475.3(FAM186A):c.4788G>C (p.Ala1596=)	FAM186A	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2642980	NM_001145475.3(FAM186A):c.4788G>T (p.Ala1596=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2341632	NM_001145475.3(FAM186A):c.4751C>T (p.Ala1584Val)	FAM186A (A1584V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2642981	NM_001145475.3(FAM186A):c.4728G>T (p.Gly1576=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2672505	NM_001145475.3(FAM186A):c.4723C>T (p.Leu1575=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642982	NM_001145475.3(FAM186A):c.4687T>C (p.Leu1563=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642983	NM_001145475.3(FAM186A):c.4680T>G (p.Ala1560=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642984	NM_001145475.3(FAM186A):c.4543T>C (p.Leu1515=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642985	NM_001145475.3(FAM186A):c.4500C>G (p.Ala1500=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642986	NM_001145475.3(FAM186A):c.4449C>G (p.Leu1483=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642987	NM_001145475.3(FAM186A):c.4362G>A (p.Glu1454=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2372540	NM_001145475.3(FAM186A):c.4335G>C (p.Met1445Ile)	FAM186A (M1445I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2642988	NM_001145475.3(FAM186A):c.4290T>C (p.Ala1430=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642989	NM_001145475.3(FAM186A):c.4284A>C (p.Ala1428=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3092166	NM_001145475.3(FAM186A):c.4263C>G (p.Ile1421Met)	FAM186A (I1421M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221661	NM_001145475.3(FAM186A):c.4255T>G (p.Leu1419Val)	FAM186A (L1419V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345252	NM_001145475.3(FAM186A):c.4253A>T (p.Glu1418Val)	FAM186A (E1418V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280431	NM_001145475.3(FAM186A):c.4238C>T (p.Pro1413Leu)	FAM186A (P1413L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092165	NM_001145475.3(FAM186A):c.4198A>G (p.Thr1400Ala)	FAM186A (T1400A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277311	NM_001145475.3(FAM186A):c.4143G>C (p.Gln1381His)	FAM186A (Q1381H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277300	NM_001145475.3(FAM186A):c.4138G>A (p.Ala1380Thr)	FAM186A (A1380T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533148	NM_001145475.3(FAM186A):c.4109C>A (p.Ala1370Asp)	FAM186A (A1370D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220498	NM_001145475.3(FAM186A):c.4109C>T (p.Ala1370Val)	FAM186A (A1370V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257517	NM_001145475.3(FAM186A):c.4102G>T (p.Ala1368Ser)	FAM186A (A1368S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292061	NM_001145475.3(FAM186A):c.4090A>G (p.Thr1364Ala)	FAM186A (T1364A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092164	NM_001145475.3(FAM186A):c.4003C>G (p.Gln1335Glu)	FAM186A (Q1335E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224439	NM_001145475.3(FAM186A):c.3995C>T (p.Ala1332Val)	FAM186A (A1332V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389210	NM_001145475.3(FAM186A):c.3985C>A (p.Pro1329Thr)	FAM186A (P1329T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092163	NM_001145475.3(FAM186A):c.3979C>A (p.Leu1327Ile)	FAM186A (L1327I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226322	NM_001145475.3(FAM186A):c.3964G>A (p.Ala1322Thr)	FAM186A (A1322T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092162	NM_001145475.3(FAM186A):c.3928G>T (p.Ala1310Ser)	FAM186A (A1310S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092161	NM_001145475.3(FAM186A):c.3899G>C (p.Gly1300Ala)	FAM186A (G1300A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277299	NM_001145475.3(FAM186A):c.3826G>T (p.Gly1276Trp)	FAM186A (G1276W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092159	NM_001145475.3(FAM186A):c.3779T>C (p.Val1260Ala)	FAM186A (V1260A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2541938	NM_001145475.3(FAM186A):c.3754G>A (p.Gly1252Arg)	FAM186A (G1252R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213781	NM_001145475.3(FAM186A):c.3734C>T (p.Pro1245Leu)	FAM186A (P1245L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244865	NM_001145475.3(FAM186A):c.3715T>G (p.Leu1239Val)	FAM186A (L1239V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229314	NM_001145475.3(FAM186A):c.3715T>A (p.Leu1239Met)	FAM186A (L1239M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325158	NM_001145475.3(FAM186A):c.3661C>T (p.Pro1221Ser)	FAM186A (P1221S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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