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Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MET
(A48T)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+6 more
GConflicting classifications of pathogenicity
MET
(A48G)
Single nucleotide variant
(intron variant +1 more)
Autosomal recessive nonsyndromic hearing loss 97
+5 more
GConflicting classifications of pathogenicity
MET
(V136I)
Single nucleotide variant
(missense variant +1 more)
MET-related disorder
+9 more
GConflicting classifications of pathogenicity
MET
(N149S)
Single nucleotide variant
(missense variant +1 more)
Osteofibrous dysplasia
+5 more
GUncertain significance
MET
(E254D)
Single nucleotide variant
(missense variant +1 more)
Papillary renal cell carcinoma type 1
+7 more
GConflicting classifications of pathogenicity
MET
(E267K)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive nonsyndromic hearing loss 97
+6 more
GUncertain significance
MET
(T273N)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive nonsyndromic hearing loss 97
+6 more
GConflicting classifications of pathogenicity
MET
(I316M)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive nonsyndromic hearing loss 97
+7 more
GBenign/Likely benign
MET
(A361S)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+5 more
GConflicting classifications of pathogenicity
MET
(L386R)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+5 more
GUncertain significance
MET
(P392T)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+6 more
GUncertain significance
MET
(I446V +1 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+6 more
GConflicting classifications of pathogenicity
MET
(D482N +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GUncertain significance
MET
(T557A +1 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+7 more
GConflicting classifications of pathogenicity
MET
(T621I +1 more)
Single nucleotide variant
(missense variant)
not provided
+6 more
GConflicting classifications of pathogenicity
MET
(G645R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
MET
(R731* +1 more)
Single nucleotide variant
(nonsense)
Renal cell carcinoma
+5 more
GUncertain significance
MET
(H810R +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+5 more
GConflicting classifications of pathogenicity
MET
(M870K +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+7 more
GConflicting classifications of pathogenicity
MET
(T913M +2 more)
Single nucleotide variant
(missense variant)
not provided
+7 more
GConflicting classifications of pathogenicity
MET
(G535S +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+5 more
GUncertain significance
MET
(I1363T +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+7 more
GConflicting classifications of pathogenicity
MET
(P1382S +2 more)
Single nucleotide variant
(missense variant)
not provided
+6 more
GUncertain significance
MET
(N1392K +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+5 more
GConflicting classifications of pathogenicity
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