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Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MET
(V37A)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer
+4 more
GBenign/Likely benign
MET
(T67A)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MET
(E168D)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GConflicting classifications of pathogenicity
MET
(S203T)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
MET
(I316M)
Single nucleotide variant
(missense variant +1 more)
not specified
+7 more
GBenign/Likely benign
MET
(S323G)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GConflicting classifications of pathogenicity
MET
(D340G)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GUncertain significance
MET
(K350Q)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
GUncertain significance
MET
(N375S)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GBenign
MET
(H394N)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
GUncertain significance
MET
(A411V)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+1 more
GConflicting classifications of pathogenicity
MET
(R413S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
MET
(M431T +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
MET
(S435N +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MET
(E436Q +1 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+1 more
GUncertain significance
MET
(D449N +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MET
Single nucleotide variant
(intron variant)
Renal cell carcinoma
GUncertain significance
MET
(L604V +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
MET
(N813D +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+2 more
GUncertain significance
MET
(R988C +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign/Likely benign
MET
(T1010I +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
MET
(G1137A +2 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
MET
(A1402G +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MET
Single nucleotide variant
not provided
GBenign
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