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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALK
(R1275Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
ALK
(I1250T +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(F1245V +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma
GPathogenic
ALK
(F1174V +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma
+1 more
GPathogenic
ALK
(T1151M +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
ALK
(G1128A +1 more)
Single nucleotide variant
(missense variant)
Neoplasm of brain
+2 more
GPathogenic/Likely pathogenic; risk factor
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