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Items: 34

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MET
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
MET
Single nucleotide variant
(synonymous variant +1 more)
Renal cell carcinoma
+4 more
GBenign
MET
Single nucleotide variant
(synonymous variant +1 more)
Renal cell carcinoma
+2 more
GConflicting classifications of pathogenicity
MET
(P97A)
Single nucleotide variant
(missense variant +1 more)
MET-related condition
+4 more
GConflicting classifications of pathogenicity
MET
Single nucleotide variant
(synonymous variant +1 more)
Renal cell carcinoma
+3 more
GBenign
MET
(E168D)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+4 more
GConflicting classifications of pathogenicity
MET
Single nucleotide variant
(synonymous variant +1 more)
Renal cell carcinoma
+5 more
GBenign
MET
Single nucleotide variant
(synonymous variant +1 more)
Renal cell carcinoma
+2 more
GBenign/Likely benign
MET
(T301A)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+4 more
GConflicting classifications of pathogenicity
MET
(I316M)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+7 more
GBenign/Likely benign
MET
(D340G)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive nonsyndromic hearing loss 97
+4 more
GUncertain significance
MET
(R359Q)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+4 more
GConflicting classifications of pathogenicity
MET
(M362T)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+4 more
GBenign
MET
(N375S)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+4 more
GBenign
MET
Single nucleotide variant
(synonymous variant +1 more)
Renal cell carcinoma
+4 more
GBenign
MET
(R469Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
MET
Single nucleotide variant
(synonymous variant)
MET-related condition
+3 more
GConflicting classifications of pathogenicity
MET
Single nucleotide variant
(synonymous variant)
Renal cell carcinoma
+4 more
GBenign
MET
(S663L +1 more)
Single nucleotide variant
(missense variant)
Ovarian cancer
+5 more
GConflicting classifications of pathogenicity
MET
Duplication
(intron variant)
not provided
GUncertain significance
MET
(Q830E +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+3 more
GConflicting classifications of pathogenicity
MET
Deletion
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
MET
(H906Y +2 more)
Single nucleotide variant
(missense variant)
MET-related condition
+3 more
GBenign/Likely benign
MET
(R988C +2 more)
Single nucleotide variant
(missense variant)
MET-related condition
+5 more
GConflicting classifications of pathogenicity
MET
(T1010I +2 more)
Single nucleotide variant
(missense variant)
MET-related condition
+7 more
GConflicting classifications of pathogenicity
MET
(P1091S +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+2 more
GConflicting classifications of pathogenicity
MET
(H1112R +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+3 more
GPathogenic
MET
(L1223V +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MET
(Y1248H +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MET
(G1270S +1 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+2 more
GUncertain significance
MET
Single nucleotide variant
(synonymous variant)
Renal cell carcinoma
+5 more
GBenign
MET
Single nucleotide variant
(synonymous variant)
Renal cell carcinoma
+5 more
GBenign
MET
Single nucleotide variant
(synonymous variant)
Renal cell carcinoma
+5 more
GBenign
MET
(D1391H +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+2 more
GConflicting classifications of pathogenicity
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