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Items: 1 to 100 of 353

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALK
(P1618S +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(K1610N +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(L1609M +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(E1605K +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(Y1604C +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
ALK
(G532R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(P1599H +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
ALK
(P1599S +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GConflicting classifications of pathogenicity
ALK
(E1594K +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(G1590S +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(Q1587L +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ALK
(N1583S +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ALK
(G1580R +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ALK
(H1576R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(R1575H +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(V1569A +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(E1568A +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(K1567N +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(L1562R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(P1551L +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(L1550P +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(R1549I +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+2 more
GConflicting classifications of pathogenicity
ALK
(T1540S +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(G1534E +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(D1529H +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(D1529N +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
Duplication
(inframe_insertion)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(K1525del +1 more)
Microsatellite
(inframe_deletion)
Neuroblastoma, susceptibility to, 3
+2 more
GConflicting classifications of pathogenicity
ALK
(A1523V +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(P1515T +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(K1514E +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(E1513K +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(R428G +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(G1494E +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(V424I +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(K423Q +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GConflicting classifications of pathogenicity
ALK
(S1481F +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(H1475Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(G406R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(P401L +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(P1469S +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(G382S +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(E1434G +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(E365Q +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(S1427P +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(V1421F +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(V1413G +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(V345M +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
ALK
(V1411A +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Deletion
(inframe_deletion)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(E1409G +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(V1405A +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(E1400D +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+2 more
GConflicting classifications of pathogenicity
ALK
(E1400A +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(I1399T +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(P1398L +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(Q1388H +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(V1358I +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(T1343I +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ALK
(S1324C +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(V249M +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(F1315S +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(T1310I +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(K1309I +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(S1308F +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(S1281N +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
ALK
(A1280V +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
ALK
(I1268F +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(V1265L +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(G195R +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(I1250T +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(D1249Y +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(R1248Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(R1231W +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
ALK
(V1229M +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(R1214C +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(P1213A +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(R1212P +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(R1212H +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(R141Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ALK
(L1208F +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(F1207S +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(G1202R +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(A1200V +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+2 more
GConflicting classifications of pathogenicity
ALK
(M1199L +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(M1199L +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(R1192W +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(P1191H +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+2 more
GUncertain significance
ALK
(S1186C +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(R1181H +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(R1181C +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(Q1177P +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(N1175S +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(E93T +1 more)
Indel
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(E1161K +1 more)
Single nucleotide variant
(missense variant)
ALK-related disorder
+3 more
GUncertain significance
ALK
(D1141N +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
ALK
(G1137R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(Q1134L +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(A1126T +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(G1121D +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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