ClinVar Miner

List of variants in gene FANCC reported as likely benign for not specified

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Gene type:
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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_000136.3(FANCC):c.77C>T (p.Ser26Phe) rs1800361 0.00511
NM_000136.3(FANCC):c.-79+5G>A rs4647350 0.00411
NM_000136.3(FANCC):c.-225C>T rs182633348 0.00262
NM_000136.3(FANCC):c.178G>A (p.Val60Ile) rs138629441 0.00091
NM_000136.3(FANCC):c.-78-18T>G rs560839822 0.00032
NM_000136.3(FANCC):c.166-7T>C rs369052148 0.00027
NM_000136.3(FANCC):c.250+16G>A rs371993188 0.00011
NM_000136.3(FANCC):c.345+6A>T rs368595927 0.00007
NM_000136.3(FANCC):c.-65C>T rs371725430 0.00006
NM_000136.3(FANCC):c.-85C>T rs876661052 0.00005
NM_000136.3(FANCC):c.-18C>G rs762660689 0.00004
NM_000136.3(FANCC):c.438T>C (p.Tyr146=) rs765990832 0.00003
NM_000136.3(FANCC):c.-41A>G rs768624552 0.00002
NM_000136.3(FANCC):c.-13C>T rs1057521107 0.00001
NM_000136.3(FANCC):c.-48G>A rs1283535718 0.00001
NM_000136.3(FANCC):c.-61C>G rs1048489323 0.00001
NM_000136.3(FANCC):c.-71G>A rs1296685064 0.00001
NM_000136.3(FANCC):c.-82C>G rs1057522510 0.00001
NM_000136.3(FANCC):c.165+10G>A rs767721720 0.00001
NM_000136.3(FANCC):c.165+12A>G rs200547296 0.00001
NM_000136.3(FANCC):c.216A>G (p.Ala72=) rs1057523069 0.00001
NM_000136.3(FANCC):c.327A>G (p.Lys109=) rs1399574459 0.00001
NM_000136.3(FANCC):c.345G>A (p.Gln115=) rs1031713372 0.00001
NM_000136.3(FANCC):c.501T>C (p.Asn167=) rs1057520284 0.00001
NM_000136.3(FANCC):c.-19C>A rs772475410
NM_000136.3(FANCC):c.-23A>G rs1057524011
NM_000136.3(FANCC):c.-35C>T rs1554858416
NM_000136.3(FANCC):c.-36G>A rs1226649340
NM_000136.3(FANCC):c.-3A>G rs1064793109
NM_000136.3(FANCC):c.-65C>G rs371725430
NM_000136.3(FANCC):c.-66C>T rs1057524245
NM_000136.3(FANCC):c.-6T>G rs1554858394
NM_000136.3(FANCC):c.-77T>C rs1057521620
NM_000136.3(FANCC):c.-78-17_-78-14del rs1064795929
NM_000136.3(FANCC):c.-78-20A>G rs1057524180
NM_000136.3(FANCC):c.-79+11G>C rs1554876653
NM_000136.3(FANCC):c.-79+13C>T rs1554876652
NM_000136.3(FANCC):c.-79+14C>G rs1057522357
NM_000136.3(FANCC):c.-84C>T rs1057522623
NM_000136.3(FANCC):c.138G>A (p.Arg46=) rs1057521212
NM_000136.3(FANCC):c.166-18T>C rs1057522385
NM_000136.3(FANCC):c.207A>G (p.Gln69=) rs1554857834
NM_000136.3(FANCC):c.250+12A>G rs1057522103
NM_000136.3(FANCC):c.251-11C>T rs1554856148
NM_000136.3(FANCC):c.270A>C (p.Leu90=) rs1057523841
NM_000136.3(FANCC):c.345+18G>C rs765413863
NM_000136.3(FANCC):c.399T>G (p.Leu133=) rs864622764
NM_000136.3(FANCC):c.456+20C>T rs1057520283
NM_000136.3(FANCC):c.457-15G>T rs1057523218
NM_000136.3(FANCC):c.516A>G (p.Gln172=) rs748322179
NM_000136.3(FANCC):c.6T>C (p.Ala2=) rs376084231
NM_000136.3(FANCC):c.90C>G (p.Thr30=) rs756684704

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