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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RET
(S891A +17 more)
Single nucleotide variant
(missense variant)
not provided
+10 more
GPathogenic
RET
(M918T +17 more)
Single nucleotide variant
(missense variant)
Medullary thyroid carcinoma
+17 more
GPathogenic/Likely pathogenic
MEN1
(P540S +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GConflicting classifications of pathogenicity
MEN1
(P499L +3 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 1
+1 more
GUncertain significance
MEN1
(E477* +3 more)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic
MEN1
(W436C +3 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
MEN1
(P412A +3 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 1
+1 more
GUncertain significance
MEN1
(R394Q +3 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 1
+1 more
GConflicting classifications of pathogenicity
MEN1
(V205A +2 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 1
GUncertain significance
MEN1
(R21S)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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