ClinVar Miner

List of variants in gene FANCC reported as uncertain significance for DNA repair disease

Included ClinVar conditions (95):
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Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP
NM_000136.2(FANCC):c.-155A>C rs549658720
NM_000136.2(FANCC):c.-172G>T rs1057515706
NM_000136.2(FANCC):c.-225C>T rs182633348
NM_000136.2(FANCC):c.-246A>G rs1000528763
NM_000136.2(FANCC):c.-2A>G rs773045474
NM_000136.2(FANCC):c.109C>G (p.His37Asp) rs864622230
NM_000136.2(FANCC):c.110A>C (p.His37Pro)
NM_000136.2(FANCC):c.112G>C (p.Val38Leu) rs778951584
NM_000136.2(FANCC):c.127G>A (p.Glu43Lys) rs374836770
NM_000136.2(FANCC):c.143T>C (p.Met48Thr)
NM_000136.2(FANCC):c.156G>C (p.Leu52Phe) rs1060502518
NM_000136.2(FANCC):c.160G>A (p.Glu54Lys)
NM_000136.2(FANCC):c.164T>C (p.Met55Thr) rs1060502513
NM_000136.2(FANCC):c.178G>A (p.Val60Ile) rs138629441
NM_000136.2(FANCC):c.191T>G (p.Phe64Cys) rs375921240
NM_000136.2(FANCC):c.202G>A (p.Gly68Ser)
NM_000136.2(FANCC):c.202G>C (p.Gly68Arg) rs777111154
NM_000136.2(FANCC):c.214G>A (p.Ala72Thr) rs567465885
NM_000136.2(FANCC):c.233C>A (p.Pro78His) rs138722298
NM_000136.2(FANCC):c.246A>G (p.Ala82=) rs1554857810
NM_000136.2(FANCC):c.248A>G (p.Tyr83Cys) rs140992397
NM_000136.2(FANCC):c.262A>C (p.Lys88Gln) rs1060502519
NM_000136.2(FANCC):c.271A>G (p.Ile91Val) rs771619614
NM_000136.2(FANCC):c.28T>G (p.Cys10Gly) rs147479204
NM_000136.2(FANCC):c.29G>A (p.Cys10Tyr) rs143152201
NM_000136.2(FANCC):c.328C>G (p.Leu110Val) rs1554856102
NM_000136.2(FANCC):c.329T>C (p.Leu110Pro) rs777731560
NM_000136.2(FANCC):c.345+6A>T rs368595927
NM_000136.2(FANCC):c.345G>A (p.Gln115=) rs1031713372
NM_000136.2(FANCC):c.34T>G (p.Tyr12Asp) rs766173332
NM_000136.2(FANCC):c.34_36delTAT (p.Tyr12del) rs1554858333
NM_000136.2(FANCC):c.38A>G (p.Gln13Arg) rs199968672
NM_000136.2(FANCC):c.395C>G (p.Ala132Gly) rs587779905
NM_000136.2(FANCC):c.397C>T (p.Leu133Phe) rs587779906
NM_000136.2(FANCC):c.3G>A (p.Met1Ile)
NM_000136.2(FANCC):c.413T>G (p.Leu138Arg)
NM_000136.2(FANCC):c.424C>G (p.Pro142Ala) rs864622581
NM_000136.2(FANCC):c.433T>C (p.Tyr145His) rs751054264
NM_000136.2(FANCC):c.436_438delTAT (p.Tyr146del) rs761347179
NM_000136.2(FANCC):c.437A>C (p.Tyr146Ser)
NM_000136.2(FANCC):c.440C>T (p.Pro147Leu) rs730881711
NM_000136.2(FANCC):c.457-10delT
NM_000136.2(FANCC):c.457-7T>C rs749994612
NM_000136.2(FANCC):c.46A>G (p.Met16Val)
NM_000136.2(FANCC):c.46A>T (p.Met16Leu) rs1390412870
NM_000136.2(FANCC):c.472G>C (p.Ala158Pro) rs372338418
NM_000136.2(FANCC):c.491A>T (p.Asn164Ile) rs950623649
NM_000136.2(FANCC):c.509A>G (p.Asn170Ser) rs749322338
NM_000136.2(FANCC):c.511A>G (p.Thr171Ala) rs1554842592
NM_000136.2(FANCC):c.521G>A (p.Arg174Gln) rs755283850
NM_000136.2(FANCC):c.522-4A>G rs371422485
NM_000136.2(FANCC):c.523A>G (p.Met175Val) rs876661083
NM_000136.2(FANCC):c.532G>A (p.Glu178Lys) rs554302947
NM_000136.2(FANCC):c.536G>A (p.Arg179Gln) rs538875706
NM_000136.2(FANCC):c.542C>T (p.Ala181Val) rs182879858
NM_000136.2(FANCC):c.549G>T (p.Leu183=) rs863224611
NM_000136.2(FANCC):c.554G>A (p.Arg185Gln) rs370346767
NM_000136.2(FANCC):c.558_563del6 (p.Cys187_Val188del) rs1554838595
NM_000136.2(FANCC):c.560G>A (p.Cys187Tyr)
NM_000136.2(FANCC):c.565C>G (p.Pro189Ala) rs377620735
NM_000136.2(FANCC):c.572T>C (p.Ile191Thr)
NM_000136.2(FANCC):c.584A>G (p.Asp195Gly) rs1800365
NM_000136.2(FANCC):c.591C>G (p.Asp197Glu) rs1457631500
NM_000136.2(FANCC):c.603G>T (p.Glu201Asp) rs1060502516
NM_000136.2(FANCC):c.607C>T (p.Leu203Phe) rs878853672
NM_000136.2(FANCC):c.620A>T (p.His207Leu) rs202038890
NM_000136.2(FANCC):c.625C>T (p.Arg209Cys) rs373270404
NM_000136.2(FANCC):c.626G>A (p.Arg209His) rs587778327
NM_000136.2(FANCC):c.632C>G (p.Pro211Arg) rs140781259
NM_000136.2(FANCC):c.652G>C (p.Glu218Gln) rs752339229
NM_000136.2(FANCC):c.668T>C (p.Val223Ala) rs751410815
NM_000136.2(FANCC):c.673G>A (p.Glu225Lys) rs374176091
NM_000136.2(FANCC):c.679A>G (p.Ile227Val) rs864622550
NM_000136.2(FANCC):c.80C>T (p.Thr27Ile)
NM_000136.2(FANCC):c.8A>C (p.Gln3Pro) rs1415268424
NM_000136.2(FANCC):c.9A>T (p.Gln3His) rs769585639

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