List of variants in gene combination AOPEP, FANCC reported by ITMI

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.1345G>A (p.Val449Met)	rs1800367	0.02254
NM_000136.3(FANCC):c.1329+175C>T	rs112446681	0.00401
NM_000136.3(FANCC):c.1394A>G (p.Gln465Arg)	rs1800368	0.00361
NM_000136.3(FANCC):c.584A>T (p.Asp195Val)	rs1800365	0.00275
NM_000136.3(FANCC):c.1156T>C (p.Ser386Pro)	rs41281202	0.00236
NM_000136.3(FANCC):c.632C>G (p.Pro211Arg)	rs140781259	0.00126
NM_000136.3(FANCC):c.1414G>A (p.Gly472Arg)	rs201063698	0.00002
NM_000136.3(FANCC):c.1063G>C (p.Asp355His)	rs587778325	0.00001
NM_000136.3(FANCC):c.1329+149G>A	rs551334290
NM_000136.3(FANCC):c.1329+181_1329+183del	rs587778328
NM_000136.3(FANCC):c.1585A>C (p.Thr529Pro)	rs587778326
NM_000136.3(FANCC):c.626G>T (p.Arg209Leu)	rs587778327

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