"KCCC/NGS Laboratory, Kuwait Cancer Control Center"[submitter] AND "FA - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 383837	NM_000136.3(FANCC):c.1560C>T (p.His520=)	AOPEP, FANCC	Single nucleotide variant (synonymous variant)	not specified +4 more	GLikely benign
Select item 182501	NM_000136.3(FANCC):c.1509G>A (p.Thr503=)	AOPEP, FANCC	Single nucleotide variant (synonymous variant)	FANCC-related condition +4 more	GConflicting classifications of pathogenicity
Select item 137285	NM_000136.3(FANCC):c.1485G>A (p.Leu495=)	FANCC, AOPEP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 134297	NM_000136.3(FANCC):c.1394A>G (p.Gln465Arg)	AOPEP, FANCC (Q465R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GBenign/Likely benign
Select item 134298	NM_000136.3(FANCC):c.1345G>A (p.Val449Met)	AOPEP, FANCC (V449M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 210976	NM_000136.3(FANCC):c.1330-3C>T	AOPEP, FANCC	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 134308	NM_000136.3(FANCC):c.1329+175C>T	AOPEP, FANCC (R463C)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GBenign
Select item 237065	NM_000136.3(FANCC):c.1200C>T (p.Phe400=)	FANCC, AOPEP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 255274	NM_000136.3(FANCC):c.1161C>T (p.Cys387=)	AOPEP, FANCC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +5 more	GLikely benign
Select item 255273	NM_000136.3(FANCC):c.1155-38T>C	AOPEP, FANCC	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 127550	NM_000136.3(FANCC):c.973G>A (p.Ala325Thr)	AOPEP, FANCC (A325T)	Single nucleotide variant (missense variant)	FANCC-related condition +5 more	GBenign/Likely benign
Select item 220920	NM_000136.3(FANCC):c.843+4C>T	AOPEP, FANCC	Single nucleotide variant (intron variant)	not specified +4 more	GBenign/Likely benign
Select item 219714	NM_000136.3(FANCC):c.609C>T (p.Leu203=)	AOPEP, FANCC	Single nucleotide variant (synonymous variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 182498	NM_000136.3(FANCC):c.457-18A>G	FANCC	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 220308	NM_000136.3(FANCC):c.438T>C (p.Tyr146=)	FANCC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 134304	NM_000136.3(FANCC):c.416G>A (p.Gly139Glu)	FANCC (G139E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GBenign/Likely benign
Select item 255275	NM_000136.3(FANCC):c.408A>G (p.Gln136=)	FANCC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 182502	NM_000136.3(FANCC):c.251-20T>C	FANCC	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 134301	NM_000136.3(FANCC):c.77C>T (p.Ser26Phe)	FANCC (S26F)	Single nucleotide variant (missense variant)	FANCC-related condition +6 more	GConflicting classifications of pathogenicity
Select item 137287	NM_000136.3(FANCC):c.-29A>C	FANCC	Single nucleotide variant (5 prime UTR variant)	not specified +2 more	GBenign

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Items: 20