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Links from MedGen

Items: 1 to 100 of 379

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MET
Single nucleotide variant
(splice donor variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
(F1134I +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
GUncertain significance
PRCC
(S241L)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
(G535S +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+5 more
GUncertain significance
MET
(L73V +1 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+1 more
GUncertain significance
MET
(T513I +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+2 more
GConflicting classifications of pathogenicity
MET
Duplication
Papillary renal cell carcinoma type 1
+1 more
GUncertain significance
MET
Deletion
Papillary renal cell carcinoma type 1
+1 more
GUncertain significance
MET
(N1392K +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+5 more
GConflicting classifications of pathogenicity
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GBenign
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
COMETT, MET
Single nucleotide variant
(5 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
COMETT, MET
Single nucleotide variant
(5 prime UTR variant)
Papillary renal cell carcinoma type 1
GBenign
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GBenign
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GBenign
MET
(E1082D +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+3 more
GUncertain significance
MET
(S283P)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GBenign
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GBenign
MET
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GConflicting classifications of pathogenicity
COMETT, MET
Single nucleotide variant
(5 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GBenign
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GBenign
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(3 prime UTR variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
(H484Y +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 97
+3 more
GUncertain significance
MET
(H855R +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
CFTR, ASZ1
+7 more
Deletion
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Duplication
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Duplication
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Duplication
Renal cell carcinoma
+1 more
GUncertain significance
MET
(N149S)
Single nucleotide variant
(missense variant +1 more)
Osteofibrous dysplasia
+5 more
GUncertain significance
MET
(D123N)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+3 more
GUncertain significance
MET
(V6L)
Single nucleotide variant
(missense variant +1 more)
Renal cell carcinoma
+3 more
GUncertain significance
MET
(D113N +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 97
+3 more
GConflicting classifications of pathogenicity
MET
(D1380E +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(intron variant)
Papillary renal cell carcinoma type 1
GLikely benign
MET
Single nucleotide variant
(synonymous variant)
Renal cell carcinoma
+2 more
GUncertain significance
MET
Single nucleotide variant
(splice acceptor variant)
Papillary renal cell carcinoma type 1
GLikely benign
MET
Deletion
(intron variant)
Autosomal recessive nonsyndromic hearing loss 97
+3 more
GBenign
MET
Single nucleotide variant
(intron variant)
not specified
+1 more
GLikely benign
MET
Single nucleotide variant
(splice acceptor variant)
Papillary renal cell carcinoma type 1
GLikely benign
MET
Single nucleotide variant
(intron variant)
Papillary renal cell carcinoma type 1
GBenign
MET
Duplication
(intron variant)
not provided
+2 more
GBenign
MET
Single nucleotide variant
(splice acceptor variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Single nucleotide variant
(splice acceptor variant)
Papillary renal cell carcinoma type 1
GLikely benign
MET
(N137S)
Single nucleotide variant
(missense variant +1 more)
Papillary renal cell carcinoma type 1
GUncertain significance
MTOR
(D297N)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MTOR
(R1009Q)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
GPathogenic
MET
Single nucleotide variant
(synonymous variant +1 more)
Papillary renal cell carcinoma type 1
+1 more
GLikely benign
MET
Single nucleotide variant
(synonymous variant +1 more)
Papillary renal cell carcinoma type 1
GLikely benign
MET
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
MET
Single nucleotide variant
(intron variant)
Papillary renal cell carcinoma type 1
+1 more
GConflicting classifications of pathogenicity
LOC107303340, VHL
(R136fs +1 more)
Deletion
(frameshift variant +1 more)
Von Hippel-Lindau syndrome
+3 more
GPathogenic
MET
(D1391G +2 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
MET
(V228A +1 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+1 more
GConflicting classifications of pathogenicity
MET
(M1049V +2 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+3 more
GUncertain significance
MET
(D990N +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+2 more
GUncertain significance
MET
(A991T +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
Duplication
Papillary renal cell carcinoma type 1
+1 more
GUncertain significance
MET
(E1365D +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
(S1349A +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+1 more
GUncertain significance
MET
(T1311S +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+3 more
GUncertain significance
MET
(E1017Q +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
(A909G +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+2 more
GUncertain significance
MET
Single nucleotide variant
(intron variant)
Papillary renal cell carcinoma type 1
+1 more
GConflicting classifications of pathogenicity
MET
Single nucleotide variant
(splice acceptor variant)
Papillary renal cell carcinoma type 1
GLikely benign
MET
(L622F +1 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
(L503Q +1 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
GUncertain significance
MET
(N499S +1 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+2 more
GConflicting classifications of pathogenicity
MET
(T309P)
Single nucleotide variant
(missense variant +1 more)
Papillary renal cell carcinoma type 1
+2 more
GUncertain significance
MET
(D243G)
Single nucleotide variant
(missense variant +1 more)
Papillary renal cell carcinoma type 1
+1 more
GUncertain significance
MET
(D190G)
Single nucleotide variant
(missense variant +1 more)
Papillary renal cell carcinoma type 1
+2 more
GUncertain significance
MET
(Q79R)
Single nucleotide variant
(missense variant +1 more)
Papillary renal cell carcinoma type 1
+1 more
GUncertain significance
MET
(V72A)
Single nucleotide variant
(missense variant +1 more)
Papillary renal cell carcinoma type 1
+3 more
GUncertain significance
MET
(N45K)
Single nucleotide variant
(missense variant +1 more)
Papillary renal cell carcinoma type 1
+2 more
GUncertain significance
MET
Duplication
Papillary renal cell carcinoma type 1
GUncertain significance
LOC126860157, LOC126860158
+45 more
Duplication
Papillary renal cell carcinoma type 1
GUncertain significance
MET
(R591Q +1 more)
Single nucleotide variant
(missense variant)
Renal cell carcinoma
+3 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
(V910I +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
MET
(I1363T +2 more)
Single nucleotide variant
(missense variant)
Papillary renal cell carcinoma type 1
+7 more
GConflicting classifications of pathogenicity
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