U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AOPEP, FANCC
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+3 more
GBenign/Likely benign
AOPEP, FANCC
(D195V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
AOPEP, FANCC
(R179*)
Single nucleotide variant
(nonsense)
Fanconi anemia
+3 more
GPathogenic/Likely pathogenic
FANCC
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+3 more
GPathogenic
FANCC
Microsatellite
(intron variant)
not specified
+3 more
GConflicting classifications of pathogenicity
FANCC
(S26F)
Single nucleotide variant
(missense variant)
FANCC-related condition
+6 more
GConflicting classifications of pathogenicity
FANCC
(C10Y)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
Format
Items per page
Sort by
Choose Destination