ClinVar Miner

List of variants in gene FANCC reported as likely benign for Hereditary cancer-predisposing syndrome

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Total variants: 70
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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.178G>A (p.Val60Ile) rs138629441 0.00091
NM_000136.3(FANCC):c.29G>A (p.Cys10Tyr) rs143152201 0.00019
NM_000136.3(FANCC):c.395C>G (p.Ala132Gly) rs587779905 0.00005
NM_000136.3(FANCC):c.111C>T (p.His37=) rs751219956 0.00003
NM_000136.3(FANCC):c.438T>C (p.Tyr146=) rs765990832 0.00003
NM_000136.3(FANCC):c.46A>T (p.Met16Leu) rs1390412870 0.00003
NM_000136.3(FANCC):c.351A>G (p.Val117=) rs754914546 0.00002
NM_000136.3(FANCC):c.473C>T (p.Ala158Val) rs776429990 0.00002
NM_000136.3(FANCC):c.15A>G (p.Ser5=) rs778408360 0.00001
NM_000136.3(FANCC):c.216A>G (p.Ala72=) rs1057523069 0.00001
NM_000136.3(FANCC):c.239T>C (p.Ile80Thr) rs4647419 0.00001
NM_000136.3(FANCC):c.291A>G (p.Leu97=) rs1216348860 0.00001
NM_000136.3(FANCC):c.321A>G (p.Gln107=) rs1441770870 0.00001
NM_000136.3(FANCC):c.327A>G (p.Lys109=) rs1399574459 0.00001
NM_000136.3(FANCC):c.436_438del (p.Tyr146del) rs761347179 0.00001
NM_000136.3(FANCC):c.468A>G (p.Ser156=) rs148616725 0.00001
NM_000136.3(FANCC):c.474G>A (p.Ala158=) rs768342908 0.00001
NM_000136.3(FANCC):c.501T>C (p.Asn167=) rs1057520284 0.00001
NM_000136.3(FANCC):c.510C>T (p.Asn170=) rs777734585 0.00001
NM_000136.3(FANCC):c.102C>T (p.Thr34=)
NM_000136.3(FANCC):c.112G>C (p.Val38Leu) rs778951584
NM_000136.3(FANCC):c.120G>A (p.Gln40=) rs905858585
NM_000136.3(FANCC):c.126G>A (p.Gln42=) rs1831173438
NM_000136.3(FANCC):c.132C>T (p.Phe44=) rs2136100617
NM_000136.3(FANCC):c.133C>T (p.Leu45=) rs1588353394
NM_000136.3(FANCC):c.147T>C (p.Tyr49=) rs1462121358
NM_000136.3(FANCC):c.166-4A>G
NM_000136.3(FANCC):c.174T>C (p.Asn58=)
NM_000136.3(FANCC):c.198A>T (p.Thr66=)
NM_000136.3(FANCC):c.204T>G (p.Gly68=) rs2136091102
NM_000136.3(FANCC):c.207A>G (p.Gln69=) rs1554857834
NM_000136.3(FANCC):c.240T>C (p.Ile80=) rs1554857813
NM_000136.3(FANCC):c.251-4G>A
NM_000136.3(FANCC):c.270A>G (p.Leu90=)
NM_000136.3(FANCC):c.27T>C (p.Ser9=) rs2136101890
NM_000136.3(FANCC):c.288T>C (p.Cys96=) rs864622349
NM_000136.3(FANCC):c.309G>A (p.Gln103=)
NM_000136.3(FANCC):c.315T>C (p.Ser105=) rs749048345
NM_000136.3(FANCC):c.316G>A (p.Gly106Arg)
NM_000136.3(FANCC):c.333C>T (p.Asn111=) rs2136048913
NM_000136.3(FANCC):c.336C>T (p.Ser112=) rs1057521125
NM_000136.3(FANCC):c.340A>G (p.Ile114Val) rs1830580247
NM_000136.3(FANCC):c.348T>C (p.Gly116=)
NM_000136.3(FANCC):c.349G>C (p.Val117Leu)
NM_000136.3(FANCC):c.351A>T (p.Val117=) rs754914546
NM_000136.3(FANCC):c.372A>G (p.Ala124=)
NM_000136.3(FANCC):c.396T>C (p.Ala132=)
NM_000136.3(FANCC):c.399T>G (p.Leu133=) rs864622764
NM_000136.3(FANCC):c.417G>A (p.Gly139=)
NM_000136.3(FANCC):c.423A>C (p.Ala141=)
NM_000136.3(FANCC):c.429A>T (p.Ile143=)
NM_000136.3(FANCC):c.42T>C (p.Phe14=) rs760653185
NM_000136.3(FANCC):c.445T>C (p.Leu149=) rs2135587533
NM_000136.3(FANCC):c.447G>A (p.Leu149=)
NM_000136.3(FANCC):c.516A>G (p.Gln172=) rs748322179
NM_000136.3(FANCC):c.520C>A (p.Arg174=)
NM_000136.3(FANCC):c.60T>C (p.Ser20=) rs2136101529
NM_000136.3(FANCC):c.63A>G (p.Val21=) rs1477321622
NM_000136.3(FANCC):c.6T>A (p.Ala2=)
NM_000136.3(FANCC):c.6T>C (p.Ala2=) rs376084231
NM_000136.3(FANCC):c.75T>G (p.Ala25=)
NM_000136.3(FANCC):c.81T>A (p.Thr27=)
NM_000136.3(FANCC):c.82T>C (p.Leu28=) rs1588353574
NM_000136.3(FANCC):c.84G>A (p.Leu28=)
NM_000136.3(FANCC):c.90C>A (p.Thr30=) rs756684704
NM_000136.3(FANCC):c.90C>G (p.Thr30=) rs756684704
NM_000136.3(FANCC):c.90C>T (p.Thr30=)
NM_000136.3(FANCC):c.96A>G (p.Gln32=)
NM_000136.3(FANCC):c.99C>T (p.Asp33=)

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