List of variants in gene combination AOPEP, FANCC reported as uncertain significance by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.*450G>A	rs149227790	0.00224
NM_000136.3(FANCC):c.934A>G (p.Ile312Val)	rs1800366	0.00051
NM_000136.3(FANCC):c.843+87T>C	rs183585118	0.00021
NM_000136.3(FANCC):c.817G>A (p.Glu273Lys)	rs143181565	0.00011
NM_000136.3(FANCC):c.974C>T (p.Ala325Val)	rs367618818	0.00006
NM_000136.3(FANCC):c.1316G>A (p.Arg439Lys)	rs730881723	0.00005
NM_000136.3(FANCC):c.*7C>T	rs372511678	0.00004
NM_000136.3(FANCC):c.1000C>T (p.Arg334Trp)	rs140348260	0.00004
NM_000136.3(FANCC):c.1544C>G (p.Thr515Ser)	rs201379302	0.00004
NM_000136.3(FANCC):c.1561G>A (p.Glu521Lys)	rs752855423	0.00004
NM_000136.3(FANCC):c.748C>A (p.Leu250Ile)	rs778966663	0.00004
NM_000136.3(FANCC):c.1643G>A (p.Arg548Gln)	rs730881729	0.00003
NM_000136.3(FANCC):c.1298G>A (p.Arg433His)	rs768676102	0.00001
NM_000136.3(FANCC):c.526G>C (p.Ala176Pro)	rs767389988	0.00001
NM_000136.3(FANCC):c.668T>C (p.Val223Ala)	rs751410815	0.00001
NM_000136.3(FANCC):c.792T>G (p.Ser264Arg)	rs730881717	0.00001
NM_000136.3(FANCC):c.851C>T (p.Ala284Val)	rs201281511	0.00001
NM_000136.3(FANCC):c.1633_1635del (p.Lys545del)	rs2134382487
NM_000136.3(FANCC):c.1655A>G (p.Lys552Arg)	rs1197938479
NM_000136.3(FANCC):c.691A>G (p.Lys231Glu)	rs1314066337
NM_000136.3(FANCC):c.901G>A (p.Ala301Thr)	rs972738983

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