ClinVar for Gene (Select 120114) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3356902	NM_001367949.2(FAT3):c.11431G>C (p.Val3811Leu)	FAT3 (V3811L)	Single nucleotide variant (missense variant)	FAT3-related disorder	GUncertain significance
Select item 3354886	NM_001367949.2(FAT3):c.11947C>G (p.Gln3983Glu)	FAT3 (Q3983E)	Single nucleotide variant (missense variant)	FAT3-related disorder	GUncertain significance
Select item 3353455	NM_001367949.2(FAT3):c.11801A>G (p.Asp3934Gly)	FAT3 (D3934G)	Single nucleotide variant (missense variant)	FAT3-related disorder	GUncertain significance
Select item 3277859	NM_001367949.2(FAT3):c.12098G>A (p.Gly4033Glu)	FAT3 (G4033E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277858	NM_001367949.2(FAT3):c.1555T>C (p.Phe519Leu)	FAT3 (F519L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277857	NM_001367949.2(FAT3):c.1979A>C (p.Asn660Thr)	FAT3 (N660T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277856	NM_001367949.2(FAT3):c.11572G>A (p.Asp3858Asn)	FAT3 (D3858N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277855	NM_001367949.2(FAT3):c.6743A>C (p.Tyr2248Ser)	FAT3 (Y2248S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277854	NM_001367949.2(FAT3):c.12323A>C (p.Glu4108Ala)	FAT3 (E4108A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277853	NM_001367949.2(FAT3):c.11198T>A (p.Met3733Lys)	FAT3 (M3733K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277852	NM_001367949.2(FAT3):c.2065G>A (p.Ala689Thr)	FAT3 (A689T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277851	NM_001367949.2(FAT3):c.1796C>T (p.Ala599Val)	FAT3 (A599V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277850	NM_001367949.2(FAT3):c.7283G>A (p.Arg2428Gln)	FAT3 (R2428Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277849	NM_001367949.2(FAT3):c.11329C>G (p.Pro3777Ala)	FAT3 (P3777A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277848	NM_001367949.2(FAT3):c.6158T>C (p.Val2053Ala)	FAT3 (V2053A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277847	NM_001367949.2(FAT3):c.7479C>G (p.Ser2493Arg)	FAT3 (S2493R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277846	NM_001367949.2(FAT3):c.10534A>G (p.Thr3512Ala)	FAT3 (T3512A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277845	NM_001367949.2(FAT3):c.9989A>G (p.Asn3330Ser)	FAT3 (N3330S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277844	NM_001367949.2(FAT3):c.6779C>T (p.Ala2260Val)	FAT3 (A2260V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277843	NM_001367949.2(FAT3):c.13696G>A (p.Glu4566Lys)	FAT3 (E4566K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277842	NM_001367949.2(FAT3):c.5077A>G (p.Ile1693Val)	FAT3 (I1693V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277841	NM_001367949.2(FAT3):c.8578G>A (p.Glu2860Lys)	FAT3 (E2860K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277840	NM_001367949.2(FAT3):c.803T>G (p.Val268Gly)	FAT3 (V268G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277839	NM_001367949.2(FAT3):c.13702G>A (p.Val4568Met)	FAT3 (V4568M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277838	NM_001367949.2(FAT3):c.3724G>A (p.Val1242Ile)	FAT3 (V1242I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277837	NM_001367949.2(FAT3):c.5611A>G (p.Ile1871Val)	FAT3 (I1871V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277836	NM_001367949.2(FAT3):c.8684C>T (p.Ala2895Val)	FAT3 (A2895V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277835	NM_001367949.2(FAT3):c.11591G>A (p.Arg3864His)	FAT3 (R3864H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277834	NM_001367949.2(FAT3):c.5492G>C (p.Gly1831Ala)	FAT3 (G1831A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277833	NM_001367949.2(FAT3):c.5197C>T (p.Arg1733Cys)	FAT3 (R1733C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277832	NM_001367949.2(FAT3):c.8092G>A (p.Val2698Ile)	FAT3 (V2698I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093182	NM_001367949.2(FAT3):c.92A>C (p.Gln31Pro)	FAT3 (Q31P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093180	NM_001367949.2(FAT3):c.9191T>C (p.Ile3064Thr)	FAT3 (I3064T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093179	NM_001367949.2(FAT3):c.8916G>T (p.Arg2972Ser)	FAT3 (R2972S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093178	NM_001367949.2(FAT3):c.8872C>T (p.Arg2958Cys)	FAT3 (R2958C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093177	NM_001367949.2(FAT3):c.8269G>A (p.Val2757Ile)	FAT3 (V2757I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3093176	NM_001367949.2(FAT3):c.7591A>G (p.Ile2531Val)	FAT3 (I2531V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093175	NM_001367949.2(FAT3):c.7562C>G (p.Thr2521Arg)	FAT3 (T2521R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093174	NM_001367949.2(FAT3):c.7314C>A (p.Asp2438Glu)	FAT3 (D2438E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093173	NM_001367949.2(FAT3):c.7228G>A (p.Gly2410Ser)	FAT3 (G2410S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093172	NM_001367949.2(FAT3):c.6447G>T (p.Leu2149Phe)	FAT3 (L2149F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093171	NM_001367949.2(FAT3):c.5704G>A (p.Val1902Ile)	FAT3 (V1902I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093170	NM_001367949.2(FAT3):c.5566A>T (p.Ser1856Cys)	FAT3 (S1856C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093169	NM_001367949.2(FAT3):c.5396G>C (p.Arg1799Pro)	FAT3 (R1799P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093168	NM_001367949.2(FAT3):c.5024A>T (p.Asp1675Val)	FAT3 (D1675V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093167	NM_001367949.2(FAT3):c.4801C>T (p.Leu1601Phe)	FAT3 (L1601F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093165	NM_001367949.2(FAT3):c.4517T>C (p.Met1506Thr)	FAT3 (M1506T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093164	NM_001367949.2(FAT3):c.4507T>C (p.Ser1503Pro)	FAT3 (S1503P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093163	NM_001367949.2(FAT3):c.4504G>A (p.Asp1502Asn)	FAT3 (D1502N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093162	NM_001367949.2(FAT3):c.4442A>G (p.Gln1481Arg)	FAT3 (Q1481R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093161	NM_001367949.2(FAT3):c.4172C>T (p.Thr1391Ile)	FAT3 (T1391I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093160	NM_001367949.2(FAT3):c.4168A>G (p.Asn1390Asp)	FAT3 (N1390D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093159	NM_001367949.2(FAT3):c.3808A>G (p.Lys1270Glu)	FAT3 (K1270E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093158	NM_001367949.2(FAT3):c.3662T>A (p.Phe1221Tyr)	FAT3 (F1221Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093157	NM_001367949.2(FAT3):c.3536C>A (p.Ser1179Tyr)	FAT3 (S1179Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093156	NM_001367949.2(FAT3):c.2588A>T (p.Asn863Ile)	FAT3 (N863I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093155	NM_001367949.2(FAT3):c.2311G>T (p.Asp771Tyr)	FAT3 (D771Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093154	NM_001367949.2(FAT3):c.1919C>T (p.Thr640Ile)	FAT3 (T640I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093153	NM_001367949.2(FAT3):c.13758G>T (p.Gln4586His)	FAT3 (Q4554H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093151	NM_001367949.2(FAT3):c.13220A>G (p.Glu4407Gly)	FAT3 (E4375G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093150	NM_001367949.2(FAT3):c.13187G>A (p.Arg4396His)	FAT3 (R4396H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093149	NM_001367949.2(FAT3):c.12922G>C (p.Asp4308His)	FAT3 (D4308H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093148	NM_001367949.2(FAT3):c.12802C>T (p.Pro4268Ser)	FAT3 (P4268S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093147	NM_001367949.2(FAT3):c.12551A>T (p.Tyr4184Phe)	FAT3 (Y4184F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093146	NM_001367949.2(FAT3):c.12449T>C (p.Val4150Ala)	FAT3 (V4150A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093145	NM_001367949.2(FAT3):c.12104G>A (p.Ser4035Asn)	FAT3 (S4035N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093144	NM_001367949.2(FAT3):c.12103A>G (p.Ser4035Gly)	FAT3 (S4035G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093143	NM_001367949.2(FAT3):c.11714T>C (p.Leu3905Ser)	FAT3 (L3905S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093142	NM_001367949.2(FAT3):c.11693G>A (p.Cys3898Tyr)	FAT3 (C3898Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093141	NM_001367949.2(FAT3):c.1153A>G (p.Ile385Val)	FAT3 (I385V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3093140	NM_001367949.2(FAT3):c.11074C>T (p.Pro3692Ser)	FAT3 (P3692S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093139	NM_001367949.2(FAT3):c.11036C>A (p.Thr3679Asn)	FAT3 (T3679N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093138	NM_001367949.2(FAT3):c.10762C>G (p.Leu3588Val)	FAT3 (L3588V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093137	NM_001367949.2(FAT3):c.10685A>T (p.Glu3562Val)	FAT3 (E3562V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093136	NM_001367949.2(FAT3):c.10511G>A (p.Arg3504Gln)	FAT3 (R3504Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093135	NM_001367949.2(FAT3):c.10255G>A (p.Val3419Ile)	FAT3 (V3419I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093134	NM_001367949.2(FAT3):c.10198G>A (p.Val3400Ile)	FAT3 (V3400I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3061447	NM_001367949.2(FAT3):c.12713C>G (p.Thr4238Arg)	FAT3 (T4238R)	Single nucleotide variant (missense variant)	FAT3-related disorder	GUncertain significance
Select item 3060987	NM_001367949.2(FAT3):c.12018G>A (p.Ala4006=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GBenign
Select item 3058515	NM_001367949.2(FAT3):c.11877C>T (p.Gly3959=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GLikely benign
Select item 3057150	NM_001367949.2(FAT3):c.3684T>C (p.Asp1228=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GBenign
Select item 3057003	NM_001367949.2(FAT3):c.13239T>C (p.Ser4413=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GLikely benign
Select item 3056919	NM_001367949.2(FAT3):c.8983C>A (p.Gln2995Lys)	FAT3 (Q2995K)	Single nucleotide variant (missense variant)	FAT3-related disorder	GBenign
Select item 3056818	NM_001367949.2(FAT3):c.12375G>A (p.Thr4125=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GLikely benign
Select item 3056140	NM_001367949.2(FAT3):c.9222T>C (p.Ser3074=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GBenign
Select item 3056107	NM_001367949.2(FAT3):c.1371G>A (p.Gln457=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GBenign
Select item 3055330	NM_001367949.2(FAT3):c.1235C>T (p.Ser412Phe)	FAT3 (S412F)	Single nucleotide variant (missense variant)	FAT3-related disorder	GBenign
Select item 3054403	NM_001367949.2(FAT3):c.4969G>T (p.Val1657Leu)	FAT3 (V1657L)	Single nucleotide variant (missense variant)	FAT3-related disorder	GLikely benign
Select item 3053972	NM_001367949.2(FAT3):c.11177G>C (p.Arg3726Thr)	FAT3 (R3726T)	Single nucleotide variant (missense variant)	FAT3-related disorder	GLikely benign
Select item 3053549	NM_001367949.2(FAT3):c.4434G>T (p.Glu1478Asp)	FAT3 (E1478D)	Single nucleotide variant (missense variant)	FAT3-related disorder	GLikely benign
Select item 3052770	NM_001367949.2(FAT3):c.1194A>C (p.Val398=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GLikely benign
Select item 3051134	NM_001367949.2(FAT3):c.9247+10A>T	FAT3	Single nucleotide variant (intron variant)	FAT3-related disorder	GLikely benign
Select item 3049958	NM_001367949.2(FAT3):c.9957A>G (p.Pro3319=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GLikely benign
Select item 3049095	NM_001367949.2(FAT3):c.4224A>T (p.Ala1408=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GBenign
Select item 3049064	NM_001367949.2(FAT3):c.8865C>T (p.Asp2955=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GBenign
Select item 3048935	NM_001367949.2(FAT3):c.1758T>G (p.Val586=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GLikely benign
Select item 3048229	NM_001367949.2(FAT3):c.1470C>T (p.Ser490=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GLikely benign
Select item 3046599	NM_001367949.2(FAT3):c.11387A>G (p.Asn3796Ser)	FAT3 (N3796S)	Single nucleotide variant (missense variant)	FAT3-related disorder	GLikely benign
Select item 3045907	NM_001367949.2(FAT3):c.6304C>T (p.Leu2102=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GBenign
Select item 3045459	NM_001367949.2(FAT3):c.4215T>C (p.Ala1405=)	FAT3	Single nucleotide variant (synonymous variant)	FAT3-related disorder	GBenign

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