U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 44

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APC
(M18K)
Single nucleotide variant
(missense variant +2 more)
Classic or attenuated familial adenomatous polyposis
+3 more
GUncertain significance
APC
(R106H +3 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 1
+5 more
GConflicting classifications of pathogenicity
APC
(S127G +3 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 1
+4 more
GConflicting classifications of pathogenicity
APC
(S130G +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
APC
(E140D +3 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 1
APC
(Q203E +3 more)
Single nucleotide variant
(missense variant +1 more)
APC-Associated Polyposis Disorders
+6 more
GConflicting classifications of pathogenicity
APC
(R232Q +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+3 more
GUncertain significance
APC
(R414C +10 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
APC
(R499G +12 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
APC
(S535F +12 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
APC
(I544T +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+5 more
GConflicting classifications of pathogenicity
APC
(A735V +12 more)
Single nucleotide variant
(missense variant)
Colorectal cancer, susceptibility to
+4 more
GConflicting classifications of pathogenicity
APC
(A766V +12 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
APC
(N813S +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
APC
(P870S +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+5 more
GBenign/Likely benign
APC
(E893K +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+4 more
GConflicting classifications of pathogenicity
APC
(D1058G +12 more)
Single nucleotide variant
(missense variant)
APC-Associated Polyposis Disorders
+6 more
GConflicting classifications of pathogenicity
APC
(D1083E +12 more)
Single nucleotide variant
(missense variant)
APC-Associated Polyposis Disorders
+3 more
GBenign/Likely benign
APC
(N1118D +12 more)
Single nucleotide variant
(missense variant)
APC-Associated Polyposis Disorders
+4 more
GBenign/Likely benign
APC
(L1129S +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+5 more
GBenign/Likely benign
APC
(E1157del +12 more)
Microsatellite
(inframe_deletion)
APC-Associated Polyposis Disorders
+6 more
GBenign/Likely benign
APC
(T1160K +12 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
APC
(F1195S +12 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
APC
(I1307K +12 more)
Single nucleotide variant
(missense variant)
Familial multiple polyposis syndrome
+8 more
GConflicting classifications of pathogenicity; association; risk factor
APC
(E1317Q +12 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GBenign/Likely benign
APC
(P1458S +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer
+8 more
GConflicting classifications of pathogenicity
APC
(T1459del +12 more)
Deletion
(inframe_deletion)
not specified
+3 more
GUncertain significance
APC
(K1462E +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+2 more
GUncertain significance
APC
(L1724V +12 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
APC
(R1742H +12 more)
Single nucleotide variant
(missense variant)
APC-Associated Polyposis Disorders
+4 more
GConflicting classifications of pathogenicity
APC
(N1798D +12 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
APC
(V1804D +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
APC
(S2242G +12 more)
Single nucleotide variant
(missense variant)
Desmoid disease, hereditary
+9 more
GConflicting classifications of pathogenicity
APC
(A2274V +12 more)
Single nucleotide variant
(missense variant)
APC-Associated Polyposis Disorders
+11 more
GBenign/Likely benign
APC
(Q2291H +12 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
APC
(P2346S +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
APC
(A2472V +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
APC
(G2502S +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+5 more
GBenign
APC
(I2573V +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
APC
(S2586I +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
APC
(E2589G +12 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
APC
(S2621C +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
APC
(V2630I +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+3 more
GConflicting classifications of pathogenicity
APC
(T2820I +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
Format
Items per page
Sort by
Choose Destination