ClinVar Miner

List of variants in gene FKTN reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP
GRCh37/hg19 9q31.2(chr9:108331166-108394748)x1
NM_006731.2(FKTN):c.-7C>G rs762110230
NM_006731.2(FKTN):c.1009G>T (p.Asp337Tyr) rs752721354
NM_006731.2(FKTN):c.1021C>T (p.Pro341Ser) rs886044385
NM_006731.2(FKTN):c.1046T>C (p.Val349Ala) rs539089647
NM_006731.2(FKTN):c.105+36_105+39del rs398123554
NM_006731.2(FKTN):c.1158A>G (p.Thr386=) rs886044528
NM_006731.2(FKTN):c.1159G>A (p.Gly387Arg) rs148975262
NM_006731.2(FKTN):c.1179G>C (p.Leu393=)
NM_006731.2(FKTN):c.1181T>C (p.Phe394Ser) rs727502849
NM_006731.2(FKTN):c.1186A>C (p.Lys396Gln) rs1477740717
NM_006731.2(FKTN):c.1215_1226del (p.Asp406_Val409del) rs1554766855
NM_006731.2(FKTN):c.1224G>T (p.Lys408Asn)
NM_006731.2(FKTN):c.1228C>A (p.His410Asn) rs146272618
NM_006731.2(FKTN):c.1249G>A (p.Glu417Lys) rs765934383
NM_006731.2(FKTN):c.1250A>T (p.Glu417Val) rs543684877
NM_006731.2(FKTN):c.1270G>A (p.Gly424Ser) rs752358445
NM_006731.2(FKTN):c.1312C>T (p.Arg438Cys) rs150852885
NM_006731.2(FKTN):c.1337A>G (p.Asn446Ser) rs374912618
NM_006731.2(FKTN):c.1337A>T (p.Asn446Ile) rs374912618
NM_006731.2(FKTN):c.1380dup (p.Tyr461fs)
NM_006731.2(FKTN):c.143T>C (p.Ile48Thr) rs886044478
NM_006731.2(FKTN):c.154A>G (p.Ser52Gly) rs1064796459
NM_006731.2(FKTN):c.165+29A>G rs374371294
NM_006731.2(FKTN):c.166-12T>A rs1419099088
NM_006731.2(FKTN):c.166-4A>G rs193922689
NM_006731.2(FKTN):c.166-9C>T rs1361772036
NM_006731.2(FKTN):c.167G>A (p.Arg56His) rs146951171
NM_006731.2(FKTN):c.180A>G (p.Lys60=) rs886042513
NM_006731.2(FKTN):c.198C>G (p.Ser66=) rs367868644
NM_006731.2(FKTN):c.21C>T (p.Asn7=) rs564632018
NM_006731.2(FKTN):c.22G>T (p.Val8Leu) rs368981218
NM_006731.2(FKTN):c.25G>T (p.Val9Phe) rs145387221
NM_006731.2(FKTN):c.293C>T (p.Thr98Ile) rs376452959
NM_006731.2(FKTN):c.296C>T (p.Ser99Leu) rs768260007
NM_006731.2(FKTN):c.301T>C (p.Cys101Arg) rs886044095
NM_006731.2(FKTN):c.30G>A (p.Leu10=) rs202047149
NM_006731.2(FKTN):c.333T>C (p.Thr111=) rs141729611
NM_006731.2(FKTN):c.342A>G (p.Ala114=) rs368598407
NM_006731.2(FKTN):c.357A>G (p.Leu119=) rs760933616
NM_006731.2(FKTN):c.366T>G (p.Asn122Lys) rs150591365
NM_006731.2(FKTN):c.369+43C>T rs398123556
NM_006731.2(FKTN):c.374G>T (p.Gly125Val) rs142783718
NM_006731.2(FKTN):c.382C>T (p.Arg128Trp) rs767026996
NM_006731.2(FKTN):c.383G>A (p.Arg128Gln) rs146049441
NM_006731.2(FKTN):c.393G>A (p.Glu131=) rs1472560195
NM_006731.2(FKTN):c.402A>T (p.Gly134=) rs780921233
NM_006731.2(FKTN):c.411C>T (p.Cys137=) rs537001725
NM_006731.2(FKTN):c.41C>T (p.Thr14Met) rs149033995
NM_006731.2(FKTN):c.437G>A (p.Arg146Gln) rs143748939
NM_006731.2(FKTN):c.439C>A (p.Leu147Ile) rs727502846
NM_006731.2(FKTN):c.443A>G (p.Asp148Gly) rs773305645
NM_006731.2(FKTN):c.445G>A (p.Gly149Arg) rs200686690
NM_006731.2(FKTN):c.448A>G (p.Ile150Val) rs886044482
NM_006731.2(FKTN):c.482A>G (p.His161Arg) rs727502848
NM_006731.2(FKTN):c.485A>G (p.Tyr162Cys) rs886044210
NM_006731.2(FKTN):c.526T>G (p.Phe176Val) rs746813994
NM_006731.2(FKTN):c.531T>A (p.His177Gln) rs534638144
NM_006731.2(FKTN):c.559G>A (p.Gly187Ser) rs1187674499
NM_006731.2(FKTN):c.58T>G (p.Phe20Val) rs1554731003
NM_006731.2(FKTN):c.626G>A (p.Arg209His) rs771109111
NM_006731.2(FKTN):c.63G>C (p.Leu21=) rs766642997
NM_006731.2(FKTN):c.648-8G>T rs754786678
NM_006731.2(FKTN):c.681G>A (p.Leu227=) rs142604625
NM_006731.2(FKTN):c.694C>T (p.Pro232Ser)
NM_006731.2(FKTN):c.699G>C (p.Lys233Asn) rs886042669
NM_006731.2(FKTN):c.703C>A (p.Pro235Thr) rs373418195
NM_006731.2(FKTN):c.706A>G (p.Met236Val) rs886042241
NM_006731.2(FKTN):c.727C>T (p.Pro243Ser) rs1564301303
NM_006731.2(FKTN):c.748T>C (p.Cys250Arg) rs398123558
NM_006731.2(FKTN):c.757A>G (p.Lys253Glu) rs886044467
NM_006731.2(FKTN):c.766C>A (p.Arg256=) rs377417974
NM_006731.2(FKTN):c.76_78TAC[2] (p.Tyr28del) rs1554731028
NM_006731.2(FKTN):c.770C>T (p.Ala257Val) rs886044660
NM_006731.2(FKTN):c.781-9T>C rs370564232
NM_006731.2(FKTN):c.802G>T (p.Val268Leu) rs878854165
NM_006731.2(FKTN):c.820C>T (p.Arg274Trp) rs558187116
NM_006731.2(FKTN):c.854C>T (p.Ala285Val) rs137951613
NM_006731.2(FKTN):c.869A>T (p.Lys290Ile) rs755092516
NM_006731.2(FKTN):c.911-8C>A rs749557617

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