List of variants in gene FANCC reported by Myriad Genetics, Inc.

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.456+4A>T	rs104886456	0.00021
NM_000136.3(FANCC):c.225T>A (p.Cys75Ter)
NM_000136.3(FANCC):c.249T>A (p.Tyr83Ter)
NM_000136.3(FANCC):c.275G>A (p.Trp92Ter)	rs1830584796
NM_000136.3(FANCC):c.282_283del (p.Cys95fs)
NM_000136.3(FANCC):c.315_316insCCCG (p.Gly106fs)
NM_000136.3(FANCC):c.323C>A (p.Ser108Ter)	rs1830581816
NM_000136.3(FANCC):c.353T>A (p.Leu118Ter)	rs1825725461
NM_000136.3(FANCC):c.464T>A (p.Leu155Ter)	rs1825652774
NM_000136.3(FANCC):c.67del (p.Asp23fs)	rs104886459

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