U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 60

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APC
(R24*)
Single nucleotide variant
(nonsense +2 more)
Familial multiple polyposis syndrome
+9 more
GPathogenic/Likely pathogenic
APC
(L103V +3 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 1
+4 more
GConflicting classifications of pathogenicity
APC
(R109Q +3 more)
Single nucleotide variant
(missense variant +1 more)
Classic or attenuated familial adenomatous polyposis
+3 more
GConflicting classifications of pathogenicity
APC
(S107A +3 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 1
+1 more
GUncertain significance
APC
(E104G +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
APC
(K150R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GConflicting classifications of pathogenicity
APC
(Q223H +3 more)
Single nucleotide variant
(missense variant +2 more)
Familial adenomatous polyposis 1
+4 more
GConflicting classifications of pathogenicity
APC
(I228V +3 more)
Single nucleotide variant
(missense variant +2 more)
Classic or attenuated familial adenomatous polyposis
+3 more
GUncertain significance
APC
(A322S +6 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 1
GUncertain significance
APC
(Q366H +6 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
APC
(R414C +10 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
GBenign
APC
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
APC
(K251R +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
GUncertain significance
APC
(S519N +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
APC
(D592G +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+4 more
GUncertain significance
APC
(A679V +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+4 more
GConflicting classifications of pathogenicity
APC
(S729L +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
APC
(A766V +12 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
APC
(R786C +12 more)
Single nucleotide variant
(missense variant)
APC-related disorder
+2 more
GUncertain significance
APC
(L808V +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
GBenign
APC
(S817P +12 more)
Single nucleotide variant
(missense variant)
Classic or attenuated familial adenomatous polyposis
+4 more
GUncertain significance
APC
(G841R +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
APC
(P865S +12 more)
Single nucleotide variant
(missense variant)
Familial multiple polyposis syndrome
+6 more
GConflicting classifications of pathogenicity
APC
(A866V +12 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
APC
(Q886H +12 more)
Single nucleotide variant
(missense variant)
Gastric adenocarcinoma and proximal polyposis of the stomach
+6 more
GConflicting classifications of pathogenicity
APC
(L904F +12 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
APC
(R819I +12 more)
Indel
(missense variant)
Familial adenomatous polyposis 1
+2 more
GConflicting classifications of pathogenicity
APC
(G980V +12 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
APC
(D1058G +12 more)
Single nucleotide variant
(missense variant)
APC-Associated Polyposis Disorders
+5 more
GConflicting classifications of pathogenicity
APC
Deletion
(frameshift variant +1 more)
Familial multiple polyposis syndrome
+5 more
GPathogenic
APC
(S1082F +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
APC
(E1157del +12 more)
Microsatellite
(inframe_deletion)
Hereditary cancer-predisposing syndrome
+6 more
GBenign/Likely benign
APC
(Y1144C +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+1 more
GUncertain significance
APC
(A1340T +12 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
APC
(V1387I +12 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
APC
(A1209fs +12 more)
Duplication
(frameshift variant)
not provided
+2 more
GPathogenic
APC
(I1554F +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
APC
(T1615I +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
APC
(R1622W +12 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
APC
(G1684E +12 more)
Single nucleotide variant
(missense variant)
not provided
+8 more
GConflicting classifications of pathogenicity
APC
(N1790del +12 more)
Microsatellite
(inframe_deletion)
Familial adenomatous polyposis 1
+3 more
GConflicting classifications of pathogenicity
APC
(L1909I +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+2 more
GUncertain significance
APC
(P2158R +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+5 more
GConflicting classifications of pathogenicity
APC
(S1927del +12 more)
Deletion
(inframe_deletion)
Familial adenomatous polyposis 1
GUncertain significance
APC
(G2209C +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+5 more
GConflicting classifications of pathogenicity
APC
(P2216S +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
APC
(R2308Q +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
APC
(P2351S +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+9 more
GConflicting classifications of pathogenicity
APC
(G2352V +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+4 more
GConflicting classifications of pathogenicity
APC
(M2244I +18 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+1 more
GUncertain significance
APC
(L2366I +12 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
APC
(S2450P +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+5 more
GConflicting classifications of pathogenicity
APC
(R2487G +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
APC
(R2423H +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+2 more
GUncertain significance
APC
(K2535Q +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+3 more
GUncertain significance
APC
(N2606D +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
APC
(V2633L +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
GUncertain significance
APC
(K2685E +12 more)
Single nucleotide variant
(missense variant)
Classic or attenuated familial adenomatous polyposis
+5 more
GConflicting classifications of pathogenicity
APC
(P2727L +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
APC
(A2777T +12 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
Format
Items per page
Sort by
Choose Destination