ClinVar for Gene (Select 121006) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3277316	NM_001145475.3(FAM186A):c.1865A>G (p.Glu622Gly)	FAM186A (E622G)	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 3277314	NM_001145475.3(FAM186A):c.5942T>A (p.Val1981Asp)	FAM186A (V1981D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277313	NM_001145475.3(FAM186A):c.3152C>T (p.Pro1051Leu)	FAM186A (P1051L)	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 3277311	NM_001145475.3(FAM186A):c.4143G>C (p.Gln1381His)	FAM186A (Q1381H)	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 3277309	NM_001145475.3(FAM186A):c.5369G>A (p.Gly1790Glu)	FAM186A (G1790E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277308	NM_001145475.3(FAM186A):c.182G>A (p.Arg61Gln)	FAM186A (R61Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277306	NM_001145475.3(FAM186A):c.71T>C (p.Ile24Thr)	FAM186A (I24T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 3277304	NM_001145475.3(FAM186A):c.2245C>T (p.Pro749Ser)	FAM186A (P749S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277303	NM_001145475.3(FAM186A):c.1977T>A (p.Ser659Arg)	FAM186A (S659R)	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 3277301	NM_001145475.3(FAM186A):c.3647G>A (p.Gly1216Glu)	FAM186A (G1216E)	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 3277299	NM_001145475.3(FAM186A):c.3826G>T (p.Gly1276Trp)	FAM186A (G1276W)	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 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 3092175	NM_001145475.3(FAM186A):c.6475A>G (p.Ile2159Val)	FAM186A (I2159V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092174	NM_001145475.3(FAM186A):c.646C>T (p.Arg216Cys)	FAM186A (R216C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092173	NM_001145475.3(FAM186A):c.632G>A (p.Arg211Gln)	FAM186A (R211Q)	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 3092170	NM_001145475.3(FAM186A):c.5462C>G (p.Ser1821Cys)	FAM186A (S1821C)	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 3092168	NM_001145475.3(FAM186A):c.4788G>C (p.Ala1596=)	FAM186A	Single nucleotide variant (synonymous variant)	not specified	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 3092165	NM_001145475.3(FAM186A):c.4198A>G (p.Thr1400Ala)	FAM186A (T1400A)	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 3092163	NM_001145475.3(FAM186A):c.3979C>A (p.Leu1327Ile)	FAM186A (L1327I)	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 3092160	NM_001145475.3(FAM186A):c.382G>A (p.Ala128Thr)	FAM186A (A128T)	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 3092158	NM_001145475.3(FAM186A):c.3653C>T (p.Pro1218Leu)	FAM186A (P1218L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092157	NM_001145475.3(FAM186A):c.3539G>T (p.Gly1180Val)	FAM186A (G1180V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092156	NM_001145475.3(FAM186A):c.3498A>C (p.Lys1166Asn)	FAM186A (K1166N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092155	NM_001145475.3(FAM186A):c.3155C>A (p.Pro1052His)	FAM186A (P1052H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3092154	NM_001145475.3(FAM186A):c.3136A>G (p.Ile1046Val)	FAM186A (I1046V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3092153	NM_001145475.3(FAM186A):c.3130G>A (p.Glu1044Lys)	FAM186A (E1044K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092152	NM_001145475.3(FAM186A):c.2983C>A (p.Pro995Thr)	FAM186A (P995T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092151	NM_001145475.3(FAM186A):c.287T>C (p.Val96Ala)	FAM186A (V96A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092150	NM_001145475.3(FAM186A):c.2858C>T (p.Ala953Val)	FAM186A (A953V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3092149	NM_001145475.3(FAM186A):c.282G>C (p.Arg94Ser)	FAM186A (R94S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092148	NM_001145475.3(FAM186A):c.2771G>A (p.Arg924Gln)	FAM186A (R924Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3092147	NM_001145475.3(FAM186A):c.2426C>T (p.Ser809Leu)	FAM186A (S809L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092146	NM_001145475.3(FAM186A):c.233A>G (p.His78Arg)	FAM186A (H78R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092145	NM_001145475.3(FAM186A):c.2323A>G (p.Ser775Gly)	FAM186A (S775G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092144	NM_001145475.3(FAM186A):c.2089C>T (p.Pro697Ser)	FAM186A (P697S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092143	NM_001145475.3(FAM186A):c.2047A>G (p.Lys683Glu)	FAM186A (K683E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092140	NM_001145475.3(FAM186A):c.1832A>G (p.His611Arg)	FAM186A (H611R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
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 2672505	NM_001145475.3(FAM186A):c.4723C>T (p.Leu1575=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2672504	NM_001145475.3(FAM186A):c.4800G>T (p.Gly1600=)	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 2642992	NM_001145475.3(FAM186A):c.3276C>T (p.Ala1092=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642991	NM_001145475.3(FAM186A):c.3621C>A (p.Leu1207=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642990	NM_001145475.3(FAM186A):c.3636T>C (p.Ala1212=)	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 2642988	NM_001145475.3(FAM186A):c.4290T>C (p.Ala1430=)	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 2642986	NM_001145475.3(FAM186A):c.4449C>G (p.Leu1483=)	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 2642984	NM_001145475.3(FAM186A):c.4543T>C (p.Leu1515=)	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 2642982	NM_001145475.3(FAM186A):c.4687T>C (p.Leu1563=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642981	NM_001145475.3(FAM186A):c.4728G>T (p.Gly1576=)	FAM186A	Single nucleotide variant (synonymous variant)	not provided	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 2642979	NM_001145475.3(FAM186A):c.*8A>G	FAM186A	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 2624404	NM_001145475.3(FAM186A):c.2168A>G (p.Gln723Arg)	FAM186A (Q723R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2619873	NM_001145475.3(FAM186A):c.5425A>G (p.Thr1809Ala)	FAM186A (T1809A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617067	NM_001145475.3(FAM186A):c.3461C>T (p.Ala1154Val)	FAM186A (A1154V)	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 2613662	NM_001145475.3(FAM186A):c.88C>G (p.Gln30Glu)	FAM186A (Q30E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611422	NM_001145475.3(FAM186A):c.1336T>G (p.Phe446Val)	FAM186A (F446V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2609311	NM_001145475.3(FAM186A):c.1973A>G (p.Glu658Gly)	FAM186A (E658G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2608273	NM_001145475.3(FAM186A):c.2026A>T (p.Ile676Leu)	FAM186A (I676L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2604839	NM_001145475.3(FAM186A):c.148A>G (p.Ile50Val)	FAM186A (I50V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
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 2601503	NM_001145475.3(FAM186A):c.5992G>A (p.Glu1998Lys)	FAM186A (E1998K)	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 2598094	NM_001145475.3(FAM186A):c.5755G>A (p.Ala1919Thr)	FAM186A (A1919T)	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 2588542	NM_001145475.3(FAM186A):c.1353G>C (p.Glu451Asp)	FAM186A (E451D)	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 2541938	NM_001145475.3(FAM186A):c.3754G>A (p.Gly1252Arg)	FAM186A (G1252R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540695	NM_001145475.3(FAM186A):c.1626G>A (p.Met542Ile)	FAM186A (M542I)	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 2532311	NM_001145475.3(FAM186A):c.1699G>T (p.Val567Leu)	FAM186A (V567L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529423	NM_001145475.3(FAM186A):c.3065G>C (p.Arg1022Pro)	FAM186A (R1022P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520890	NM_001145475.3(FAM186A):c.2726A>T (p.Gln909Leu)	FAM186A (Q909L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520889	NM_001145475.3(FAM186A):c.2724G>T (p.Lys908Asn)	FAM186A (K908N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516883	NM_001145475.3(FAM186A):c.1654C>T (p.Arg552Cys)	FAM186A (R552C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516495	NM_001145475.3(FAM186A):c.1610G>A (p.Ser537Asn)	FAM186A (S537N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515872	NM_001145475.3(FAM186A):c.849C>A (p.Asn283Lys)	FAM186A (N283K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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