ClinVar Miner

List of variants in gene FLCN reported as pathogenic for Hereditary cancer-predisposing syndrome

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Total variants: 58
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HGVS dbSNP
NM_144997.7(FLCN):c.1014del (p.Trp338fs) rs1131690830
NM_144997.7(FLCN):c.1021del (p.Arg341fs) rs1060502368
NM_144997.7(FLCN):c.1062+1G>A rs1131690832
NM_144997.7(FLCN):c.1098_1102dup (p.Val368fs) rs1131690831
NM_144997.7(FLCN):c.1117C>T (p.Gln373Ter) rs398124524
NM_144997.7(FLCN):c.1153del (p.Gln385fs) rs1555607960
NM_144997.7(FLCN):c.1177-5_1177-3del rs767671406
NM_144997.7(FLCN):c.1179del (p.Met394fs) rs398124525
NM_144997.7(FLCN):c.1213dup (p.Tyr405fs) rs1131690837
NM_144997.7(FLCN):c.1215C>G (p.Tyr405Ter) rs786202541
NM_144997.7(FLCN):c.1252del (p.Leu418fs) rs864622651
NM_144997.7(FLCN):c.1285del (p.His429fs) rs80338682
NM_144997.7(FLCN):c.1285dup (p.His429fs) rs80338682
NM_144997.7(FLCN):c.1286_1287dup (p.Val430fs) rs1555607640
NM_144997.7(FLCN):c.1300+1G>A rs879255676
NM_144997.7(FLCN):c.1302_1303dup (p.Phe435fs) rs1131690829
NM_144997.7(FLCN):c.1305del (p.Phe435fs) rs398124527
NM_144997.7(FLCN):c.1318_1334dup (p.Leu449fs) rs879255677
NM_144997.7(FLCN):c.1352del (p.Pro451fs) rs1131690828
NM_144997.7(FLCN):c.1357_1363del (p.Gly453fs) rs1131690841
NM_144997.7(FLCN):c.1375_1376TC[2] (p.Leu460fs) rs1064793128
NM_144997.7(FLCN):c.1389C>A (p.Tyr463Ter) rs137852929
NM_144997.7(FLCN):c.1389C>G (p.Tyr463Ter) rs137852929
NM_144997.7(FLCN):c.1426dup (p.Asp476fs) rs1131690835
NM_144997.7(FLCN):c.1429C>T (p.Arg477Ter) rs879255678
NM_144997.7(FLCN):c.1432+1G>A rs755959303
NM_144997.7(FLCN):c.1459G>T (p.Glu487Ter) rs786202475
NM_144997.7(FLCN):c.158del (p.Gln53fs) rs1131690825
NM_144997.7(FLCN):c.189del (p.Ala64fs) rs876660611
NM_144997.7(FLCN):c.199del (p.Ala67fs) rs1555611438
NM_144997.7(FLCN):c.214del (p.Ser72fs) rs1131690824
NM_144997.7(FLCN):c.235_238del (p.Ser79fs) rs750146811
NM_144997.7(FLCN):c.250-1G>A rs786202081
NM_144997.7(FLCN):c.250-2A>G rs398124533
NM_144997.7(FLCN):c.296del (p.Asp99fs) rs398124534
NM_144997.7(FLCN):c.319_320delinsCAC (p.Val107fs) rs398124535
NM_144997.7(FLCN):c.33C>A (p.Cys11Ter) rs754616167
NM_144997.7(FLCN):c.346C>T (p.Gln116Ter) rs398124536
NM_144997.7(FLCN):c.347dup (p.Leu117fs) rs776896550
NM_144997.7(FLCN):c.3del (p.Met1fs) rs1131690838
NM_144997.7(FLCN):c.44dup (p.Arg17fs) rs1131690839
NM_144997.7(FLCN):c.466_468TTC[1] (p.Phe157del) rs786203218
NM_144997.7(FLCN):c.499C>T (p.Gln167Ter) rs587782069
NM_144997.7(FLCN):c.503_518delinsATCAG (p.Arg168fs) rs1064792959
NM_144997.7(FLCN):c.557G>A (p.Trp186Ter) rs876658409
NM_144997.7(FLCN):c.584del (p.Gly195fs) rs878855217
NM_144997.7(FLCN):c.59del (p.Phe20fs) rs876658390
NM_144997.7(FLCN):c.603_607del (p.Lys203fs) rs1131690836
NM_144997.7(FLCN):c.619-1G>A rs1131690840
NM_144997.7(FLCN):c.779+1G>C rs758175953
NM_144997.7(FLCN):c.779+1G>T rs758175953
NM_144997.7(FLCN):c.780G>A (p.Trp260Ter) rs1131690826
NM_144997.7(FLCN):c.838G>T (p.Glu280Ter) rs1060502367
NM_144997.7(FLCN):c.875T>G (p.Leu292Ter) rs879255668
NM_144997.7(FLCN):c.890_893del (p.Glu297fs) rs398124541
NM_144997.7(FLCN):c.919G>T (p.Glu307Ter) rs932256543
NM_144997.7(FLCN):c.927_954dup (p.Gly319fs) rs398124542
NM_144997.7(FLCN):c.943G>T (p.Glu315Ter) rs587781952

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