ClinVar Miner

List of variants reported as pathogenic by Center for Medical Genetics Ghent, University of Ghent

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ClinVar version:
Total variants: 200
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HGVS dbSNP gnomAD frequency
NM_000256.3(MYBPC3):c.2373dup (p.Trp792fs) rs397515963 0.00002
NM_000256.3(MYBPC3):c.2827C>T (p.Arg943Ter) rs387907267 0.00002
NM_007046.4(EMILIN1):c.119dup (p.Ser40fs) rs758895857 0.00002
NM_018699.4(PRDM5):c.247C>T (p.Arg83Cys) rs761027478 0.00002
NM_000057.4(BLM):c.3020-258A>G rs1301751251 0.00001
NM_000138.5(FBN1):c.1693C>T (p.Arg565Ter) rs113422242 0.00001
NM_000257.4(MYH7):c.428G>A (p.Arg143Gln) rs397516209 0.00001
NM_018699.4(PRDM5):c.974del (p.Cys325fs) rs766853150 0.00001
NM_000057.4(BLM):c.3379C>T (p.Gln1127Ter) rs1897212605
NM_000138.4(FBN1):c.305_306delinsAA (p.Cys102Ter) rs1555405530
NM_000138.4(FBN1):c.5225_5249del rs1555396635
NM_000138.5(FBN1):c.1066del (p.Met356fs) rs1555400609
NM_000138.5(FBN1):c.1090C>T (p.Arg364Ter) rs794728165
NM_000138.5(FBN1):c.1156_1167del (p.Asn386_Cys389del) rs672601352
NM_000138.5(FBN1):c.124del (p.Ala42fs) rs1555407414
NM_000138.5(FBN1):c.1270C>T (p.Gln424Ter) rs1439533354
NM_000138.5(FBN1):c.1318G>T (p.Glu440Ter) rs1555400406
NM_000138.5(FBN1):c.1360C>T (p.Gln454Ter) rs1555400387
NM_000138.5(FBN1):c.1422del (p.Cys474fs) rs1555400379
NM_000138.5(FBN1):c.1468+5G>A rs397515757
NM_000138.5(FBN1):c.1510T>C (p.Cys504Arg) rs1555400288
NM_000138.5(FBN1):c.1511G>A (p.Cys504Tyr) rs1156747241
NM_000138.5(FBN1):c.1546C>T (p.Arg516Ter) rs113812345
NM_000138.5(FBN1):c.1552G>T (p.Gly518Ter) rs794728168
NM_000138.5(FBN1):c.1575del (p.Thr526fs) rs1555400268
NM_000138.5(FBN1):c.1579G>T (p.Glu527Ter) rs1555400267
NM_000138.5(FBN1):c.1585C>T (p.Arg529Ter) rs137854476
NM_000138.5(FBN1):c.164+1G>A rs794728213
NM_000138.5(FBN1):c.164+1del rs1555407399
NM_000138.5(FBN1):c.1709G>A (p.Cys570Tyr) rs1555400049
NM_000138.5(FBN1):c.1715-1G>A rs1555399977
NM_000138.5(FBN1):c.1760G>A (p.Cys587Tyr) rs1555399963
NM_000138.5(FBN1):c.1794C>G (p.Cys598Trp) rs1555399954
NM_000138.5(FBN1):c.1801G>T (p.Gly601Ter) rs1555399953
NM_000138.5(FBN1):c.1837+1G>A rs397515762
NM_000138.5(FBN1):c.1837+2T>C rs1555399940
NM_000138.5(FBN1):c.1960+1G>C rs1555399804
NM_000138.5(FBN1):c.2114-1G>C rs1555399484
NM_000138.5(FBN1):c.2243del (p.Cys748fs) rs1555399371
NM_000138.5(FBN1):c.2327G>A (p.Cys776Tyr) rs1555399273
NM_000138.5(FBN1):c.2341T>A (p.Cys781Ser) rs397515766
NM_000138.5(FBN1):c.2341T>C (p.Cys781Arg) rs397515766
NM_000138.5(FBN1):c.2342G>A (p.Cys781Tyr) rs1555399271
NM_000138.5(FBN1):c.2369G>A (p.Cys790Tyr) rs193922188
NM_000138.5(FBN1):c.2412_2413del (p.Thr804_Cys805insTer) rs397515769
NM_000138.5(FBN1):c.2433C>A (p.Cys811Ter) rs193921256
NM_000138.5(FBN1):c.2433C>G (p.Cys811Trp) rs193921256
NM_000138.5(FBN1):c.2434G>T (p.Glu812Ter) rs201778577
NM_000138.5(FBN1):c.2446T>C (p.Cys816Arg) rs1555399206
NM_000138.5(FBN1):c.247+1G>T rs25404
NM_000138.5(FBN1):c.2489G>A (p.Cys830Tyr) rs397515774
NM_000138.5(FBN1):c.255C>A (p.Cys85Ter) rs1555405536
NM_000138.5(FBN1):c.2562G>A (p.Trp854Ter) rs1555399164
NM_000138.5(FBN1):c.2581C>T (p.Arg861Ter) rs140583
NM_000138.5(FBN1):c.2586dup (p.Glu863Ter) rs1555399160
NM_000138.5(FBN1):c.2657_2667del (p.Pro886fs) rs1555399146
NM_000138.5(FBN1):c.2682del (p.Ile895fs) rs193922194
NM_000138.5(FBN1):c.2737G>T (p.Glu913Ter) rs1555398996
NM_000138.5(FBN1):c.2777G>A (p.Cys926Tyr) rs1555398989
NM_000138.5(FBN1):c.2793del (p.Ser932fs) rs778900586
NM_000138.5(FBN1):c.2849G>T (p.Cys950Phe) rs1555398974
NM_000138.5(FBN1):c.3012C>A (p.Tyr1004Ter) rs397515784
NM_000138.5(FBN1):c.3012C>G (p.Tyr1004Ter) rs397515784
NM_000138.5(FBN1):c.3132C>A (p.Cys1044Ter) rs1555398677
NM_000138.5(FBN1):c.3143T>C (p.Ile1048Thr) rs1555398673
NM_000138.5(FBN1):c.3164G>A (p.Cys1055Tyr) rs397515786
NM_000138.5(FBN1):c.3202T>C (p.Cys1068Arg) rs1293095681
NM_000138.5(FBN1):c.3235_3239del (p.Asp1079fs) rs1555398642
NM_000138.5(FBN1):c.3256T>C (p.Cys1086Arg) rs1555398637
NM_000138.5(FBN1):c.3303T>A (p.Tyr1101Ter) rs1555398624
NM_000138.5(FBN1):c.3347_3348del (p.Glu1116fs) rs1555398580
NM_000138.5(FBN1):c.3373C>T (p.Arg1125Ter) rs727505006
NM_000138.5(FBN1):c.3388del (p.His1130fs) rs1555398572
NM_000138.5(FBN1):c.3458G>A (p.Cys1153Tyr) rs140599
NM_000138.5(FBN1):c.3476G>A (p.Cys1159Tyr) rs1555398524
NM_000138.5(FBN1):c.3513C>G (p.Cys1171Trp) rs775417975
NM_000138.5(FBN1):c.3539G>A (p.Cys1180Tyr) rs1555398513
NM_000138.5(FBN1):c.3559dup (p.His1187fs) rs1555398508
NM_000138.5(FBN1):c.3589+1G>T rs1555398501
NM_000138.5(FBN1):c.3623del (p.Cys1208fs) rs1555398407
NM_000138.5(FBN1):c.3795T>A (p.Cys1265Ter) rs1555398278
NM_000138.5(FBN1):c.3849del (p.Glu1283fs) rs1555398174
NM_000138.5(FBN1):c.4049G>A (p.Cys1350Tyr) rs1555397718
NM_000138.5(FBN1):c.408C>A (p.Cys136Ter) rs1555405039
NM_000138.5(FBN1):c.4099T>C (p.Cys1367Arg) rs1555397670
NM_000138.5(FBN1):c.4210+1G>A rs730880106
NM_000138.5(FBN1):c.4259G>A (p.Cys1420Tyr) rs397515804
NM_000138.5(FBN1):c.4259G>T (p.Cys1420Phe) rs397515804
NM_000138.5(FBN1):c.4285T>A (p.Cys1429Ser) rs1555397546
NM_000138.5(FBN1):c.4286G>A (p.Cys1429Tyr) rs1555397545
NM_000138.5(FBN1):c.4287T>G (p.Cys1429Trp) rs1555397543
NM_000138.5(FBN1):c.4293C>A (p.Cys1431Ter) rs112375043
NM_000138.5(FBN1):c.4337-1G>T rs1555397424
NM_000138.5(FBN1):c.4349G>A (p.Cys1450Tyr) rs1555397419
NM_000138.5(FBN1):c.4405del (p.Arg1469fs) rs794728308
NM_000138.5(FBN1):c.443del (p.Pro148fs) rs1555404820
NM_000138.5(FBN1):c.4490G>C (p.Cys1497Ser) rs1555397212
NM_000138.5(FBN1):c.4501_4511del (p.Asn1501fs) rs1555397210
NM_000138.5(FBN1):c.4539C>G (p.Cys1513Trp) rs1555397203
NM_000138.5(FBN1):c.4567C>T (p.Arg1523Ter) rs397515812
NM_000138.5(FBN1):c.4582+2T>G rs1555397193
NM_000138.5(FBN1):c.4615C>T (p.Arg1539Ter) rs111231312
NM_000138.5(FBN1):c.4621C>T (p.Arg1541Ter) rs794728228
NM_000138.5(FBN1):c.4665_4668del (p.Gly1556fs) rs1555397160
NM_000138.5(FBN1):c.4770_4771del (p.Gly1591fs) rs1555397022
NM_000138.5(FBN1):c.4786C>T (p.Arg1596Ter) rs113871094
NM_000138.5(FBN1):c.4888C>T (p.Gln1630Ter) rs794728231
NM_000138.5(FBN1):c.4898G>A (p.Cys1633Tyr) rs1555396993
NM_000138.5(FBN1):c.4914C>A (p.Tyr1638Ter) rs1555396991
NM_000138.5(FBN1):c.4926_4927del (p.Arg1644fs) rs1555396990
NM_000138.5(FBN1):c.4930C>T (p.Arg1644Ter) rs140630
NM_000138.5(FBN1):c.4943-1G>A rs1555396863
NM_000138.5(FBN1):c.4974_4975del (p.Cys1658fs) rs1555396858
NM_000138.5(FBN1):c.5015G>C (p.Cys1672Ser) rs140627
NM_000138.5(FBN1):c.5208T>A (p.Cys1736Ter) rs794728234
NM_000138.5(FBN1):c.5213_5217del (p.Ile1738fs) rs1555396757
NM_000138.5(FBN1):c.5244_5245del (p.Cys1748fs) rs1555396636
NM_000138.5(FBN1):c.5297-1G>A rs1555396435
NM_000138.5(FBN1):c.5330G>A (p.Cys1777Tyr) rs1060501069
NM_000138.5(FBN1):c.5368C>T (p.Arg1790Ter) rs113249837
NM_000138.5(FBN1):c.5371T>C (p.Cys1791Arg) rs1555396427
NM_000138.5(FBN1):c.5373T>G (p.Cys1791Trp) rs1555396426
NM_000138.5(FBN1):c.5377T>A (p.Cys1793Ser) rs1555396424
NM_000138.5(FBN1):c.538+2T>C rs1555404799
NM_000138.5(FBN1):c.5470_5483dup (p.Gly1829fs) rs1555396202
NM_000138.5(FBN1):c.5493C>G (p.Tyr1831Ter) rs1555396201
NM_000138.5(FBN1):c.5503T>A (p.Cys1835Ser) rs1555396198
NM_000138.5(FBN1):c.5520del (p.Phe1841fs) rs1555396188
NM_000138.5(FBN1):c.5557T>A (p.Cys1853Ser) rs1555395990
NM_000138.5(FBN1):c.5558G>C (p.Cys1853Ser) rs1555395989
NM_000138.5(FBN1):c.5612_5613del (p.Ser1871fs) rs1555395981
NM_000138.5(FBN1):c.5635_5636del (p.Gly1879fs) rs1555395978
NM_000138.5(FBN1):c.5684del (p.Cys1895fs) rs1555395846
NM_000138.5(FBN1):c.5688_5689del (p.Asp1898fs) rs1555395843
NM_000138.5(FBN1):c.5699G>A (p.Cys1900Tyr) rs794728237
NM_000138.5(FBN1):c.5699G>T (p.Cys1900Phe) rs794728237
NM_000138.5(FBN1):c.5809G>T (p.Gly1937Ter) rs1555395766
NM_000138.5(FBN1):c.5863C>T (p.Gln1955Ter) rs363807
NM_000138.5(FBN1):c.5863del (p.Gln1955fs) rs1555395753
NM_000138.5(FBN1):c.5898del (p.Asp1967fs) rs1555395747
NM_000138.5(FBN1):c.5961dup (p.Thr1988fs) rs1555395653
NM_000138.5(FBN1):c.6064G>T (p.Glu2022Ter) rs1555395482
NM_000138.5(FBN1):c.6160C>T (p.Gln2054Ter) rs1555395456
NM_000138.5(FBN1):c.6169C>T (p.Arg2057Ter) rs763091520
NM_000138.5(FBN1):c.6325C>T (p.Gln2109Ter) rs1555395229
NM_000138.5(FBN1):c.6388G>T (p.Glu2130Ter) rs794728334
NM_000138.5(FBN1):c.643C>T (p.Arg215Ter) rs111687884
NM_000138.5(FBN1):c.6496+2T>G rs1555395187
NM_000138.5(FBN1):c.6583G>T (p.Gly2195Ter) rs886038976
NM_000138.5(FBN1):c.660_661del (p.Pro220_Cys221insTer) rs1555401679
NM_000138.5(FBN1):c.6616+1G>A rs1064793980
NM_000138.5(FBN1):c.6658C>T (p.Arg2220Ter) rs113001196
NM_000138.5(FBN1):c.6693del (p.Lys2231fs) rs1555394901
NM_000138.5(FBN1):c.6761del (p.Gly2254fs) rs1555394780
NM_000138.5(FBN1):c.680_690del (p.Gln227fs) rs1555401671
NM_000138.5(FBN1):c.6886del (p.Gln2296fs) rs1555394641
NM_000138.5(FBN1):c.6920G>C (p.Cys2307Ser) rs137854457
NM_000138.5(FBN1):c.7039_7040del (p.Met2347fs) rs794728319
NM_000138.5(FBN1):c.7058del (p.Ser2353fs) rs1555394574
NM_000138.5(FBN1):c.7082C>A (p.Ser2361Ter) rs397515844
NM_000138.5(FBN1):c.7141C>T (p.Gln2381Ter) rs869025414
NM_000138.5(FBN1):c.7151_7152del (p.Val2384fs) rs869025423
NM_000138.5(FBN1):c.7167_7168del (p.Cys2390fs) rs397515846
NM_000138.5(FBN1):c.7180C>T (p.Arg2394Ter) rs397515848
NM_000138.5(FBN1):c.7240C>T (p.Arg2414Ter) rs112550005
NM_000138.5(FBN1):c.7323del (p.Cys2442fs) rs1555394436
NM_000138.5(FBN1):c.7398C>A (p.Tyr2466Ter) rs1555394402
NM_000138.5(FBN1):c.7432G>T (p.Glu2478Ter) rs537570299
NM_000138.5(FBN1):c.7448G>C (p.Cys2483Ser) rs1555394390
NM_000138.5(FBN1):c.772C>T (p.Gln258Ter) rs146348130
NM_000138.5(FBN1):c.7780C>T (p.Gln2594Ter) rs1555394144
NM_000138.5(FBN1):c.7780del (p.Gln2594fs) rs1555394146
NM_000138.5(FBN1):c.7813dup (p.Cys2605fs) rs1555394138
NM_000138.5(FBN1):c.7974dup (p.Cys2659fs) rs1555393848
NM_000138.5(FBN1):c.8080C>T (p.Arg2694Ter) rs200309328
NM_000138.5(FBN1):c.8149G>T (p.Glu2717Ter) rs187553035
NM_000138.5(FBN1):c.8154dup (p.Lys2719Ter) rs794728321
NM_000138.5(FBN1):c.8536G>T (p.Glu2846Ter) rs1555393508
NM_000138.5(FBN1):c.960C>A (p.Tyr320Ter) rs1555401004
NM_000138.5(FBN1):c.989-1G>C rs1555400616
NM_000256.3(MYBPC3):c.1928-2A>G rs397515937
NM_000256.3(MYBPC3):c.332_335dup (p.Glu112delinsAspTer) rs886037901
NM_000256.3(MYBPC3):c.676_701dup (p.Gly235fs) rs786204329
NM_000257.4(MYH7):c.2710C>T (p.Arg904Cys) rs727503253
NM_001035.3(RYR2):c.527G>A (p.Arg176Gln) rs794728708
NM_001039348.3(EFEMP1):c.1201C>T (p.Arg401Ter) rs2104369155
NM_001276345.2(TNNT2):c.451C>T (p.Arg151Trp) rs74315379
NM_001367624.2(ZNF469):c.1444del (p.Leu482fs) rs1484586294
NM_001367624.2(ZNF469):c.3307C>T (p.Gln1103Ter) rs1906110243
NM_001844.5(COL2A1):c.1191_1199dup (p.Ser400_Gly402dup) rs672601355
NM_001844.5(COL2A1):c.3357_3358insCT (p.Glu1120fs) rs672601354
NM_004183.4(BEST1):c.172_173dup (p.Gln58fs) rs672601356
NM_004387.4(NKX2-5):c.768T>G (p.Tyr256Ter) rs104893907
NM_007046.4(EMILIN1):c.151del (p.Arg51fs)
NM_007046.4(EMILIN1):c.1606C>T (p.Gln536Ter)
NM_007046.4(EMILIN1):c.2457_2482dup (p.Gln828fs)
NM_007046.4(EMILIN1):c.831dup (p.Ala278fs)
NM_023067.4(FOXL2):c.142_173delinsGCGCT (p.Lys48_Ser58delinsAlaLeu) rs672601357
NM_023067.4(FOXL2):c.843_859dup (p.Pro287fs) rs672601359
NM_023067.4(FOXL2):c.965_983dup (p.Thr329fs) rs672601358

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