List of variants in gene combination AOPEP, FANCC reported as benign for not specified

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.1155-38T>C	rs4647534	0.48457
NM_000136.3(FANCC):c.1345G>A (p.Val449Met)	rs1800367	0.02254
NM_000136.3(FANCC):c.843+4C>T	rs4647506	0.01468
NM_000136.3(FANCC):c.1330-3C>T	rs4647542	0.00811
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.840G>A (p.Ser280=)	rs34671520	0.00154
NM_000136.3(FANCC):c.816C>T (p.Ile272=)	rs55719336	0.00074
NM_000136.3(FANCC):c.1329+212C>T	rs41281200	0.00061
NM_000136.3(FANCC):c.1329+111C>T	rs527823099	0.00056
NM_000136.3(FANCC):c.672C>T (p.Asn224=)	rs150647141	0.00046
NM_000136.3(FANCC):c.705C>T (p.Pro235=)	rs141828876	0.00046
NM_000136.3(FANCC):c.*5C>T	rs117175949	0.00033
NM_000136.3(FANCC):c.973G>A (p.Ala325Thr)	rs201407189	0.00028
NM_000136.3(FANCC):c.1407G>A (p.Thr469=)	rs79722116	0.00020
NM_000136.3(FANCC):c.1290C>T (p.Tyr430=)	rs766105286	0.00011
NM_000136.3(FANCC):c.1509G>A (p.Thr503=)	rs144278080	0.00011
NM_000136.3(FANCC):c.522-4A>G	rs371422485	0.00011
NM_000136.3(FANCC):c.1073-5C>T	rs375613884	0.00009
NM_000136.3(FANCC):c.531C>T (p.Pro177=)	rs150070473	0.00007
NM_000136.3(FANCC):c.1242G>A (p.Ser414=)	rs587780939	0.00006
NM_000136.3(FANCC):c.*7C>T	rs372511678	0.00004
NM_000136.3(FANCC):c.897-19C>T	rs368830981	0.00002
NM_000136.3(FANCC):c.687-15A>C	rs765327075	0.00001
NM_000136.3(FANCC):c.*42G>A	rs7029888
NM_000136.3(FANCC):c.1485G>A (p.Leu495=)	rs56082100
NM_000136.3(FANCC):c.816C>G (p.Ile272Met)	rs55719336

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