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Items: 23

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RET
(L56M)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
RET
(R67H)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+8 more
GBenign/Likely benign
RET
(D102N)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+7 more
GConflicting classifications of pathogenicity
RET
(R114H)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+8 more
GBenign/Likely benign
RET
(R163Q +1 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+6 more
GConflicting classifications of pathogenicity
RET
(T278N +3 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+8 more
GBenign/Likely benign
RET
(V38M +2 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+9 more
GConflicting classifications of pathogenicity
RET
(T350I +3 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+1 more
GUncertain significance
RET
(A386V +6 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
RET
(G446R +8 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+9 more
GBenign/Likely benign
RET
(R475Q +8 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+4 more
GUncertain significance
RET
(E480K +8 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia type 2B
+4 more
GConflicting classifications of pathogenicity
RET
(D489N +8 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia type 2B
+5 more
GBenign/Likely benign
RET
(R525W +12 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+8 more
GUncertain significance
RET
(S395L +13 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+8 more
GConflicting classifications of pathogenicity
RET
(G437S +16 more)
Single nucleotide variant
(missense variant)
not provided
+9 more
GConflicting classifications of pathogenicity
RET
(T754M +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
RET
(N783T +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia type 2A
+5 more
GConflicting classifications of pathogenicity
RET
(S811C +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia type 2A
+2 more
GUncertain significance
RET
(R959W +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia type 2A
+4 more
GUncertain significance
RET
(R982C +17 more)
Single nucleotide variant
(missense variant)
not provided
+11 more
GConflicting classifications of pathogenicity
RET
(P1039Q +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+1 more
GUncertain significance
RET
(Y1062C +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
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