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Items: 20

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALK
(A1601T +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
ALK
(S1560fs +1 more)
Deletion
(frameshift variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(R1414K +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(P1398L +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ALK
(R1084H +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(R1060C)
Single nucleotide variant
(5 prime UTR variant +1 more)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(G1054S)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
+3 more
GBenign/Likely benign
ALK
Single nucleotide variant
(intron variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
+2 more
GBenign/Likely benign
ALK
(G667R)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(M596T)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+2 more
GConflicting classifications of pathogenicity
ALK
(E576*)
Single nucleotide variant
(nonsense)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(V448D)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(R395H)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
ALK
(R395C)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GConflicting classifications of pathogenicity
ALK
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign/Likely benign
ALK
(F168S)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(R133C)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(P104S)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
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