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Items: 48

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RET
Microsatellite
(inframe_indel +1 more)
not specified
+8 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(synonymous variant +1 more)
not specified
+4 more
GBenign
RET
(L56M)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+8 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2
+2 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+9 more
GBenign/Likely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
not specified
+8 more
GBenign/Likely benign
RET
Single nucleotide variant
(synonymous variant +2 more)
Hereditary cancer-predisposing syndrome
+7 more
GBenign/Likely benign
RET
(P259L +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
RET
Deletion
(intron variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
+5 more
GBenign
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia
+8 more
GConflicting classifications of pathogenicity
RET
(L375Q +6 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+5 more
GConflicting classifications of pathogenicity
RET
(A386V +6 more)
Single nucleotide variant
(missense variant)
RET-related condition
+4 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia
+8 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(intron variant)
Familial medullary thyroid carcinoma
+10 more
GBenign/Likely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+9 more
GBenign
RET
(S434G +8 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+7 more
GUncertain significance
RET
(G446R +8 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia
+9 more
GBenign/Likely benign
RET
(L452I +8 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+3 more
GConflicting classifications of pathogenicity
RET
(D567N +12 more)
Single nucleotide variant
(missense variant)
RET-related condition
+10 more
GConflicting classifications of pathogenicity
RET
(G568S +12 more)
Single nucleotide variant
(missense variant)
Familial medullary thyroid carcinoma
+7 more
GConflicting classifications of pathogenicity
RET
(R346Q +11 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RET
(C609Y +12 more)
Single nucleotide variant
(missense variant)
RET-related condition
+6 more
GPathogenic
RET
(C618R +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GPathogenic
RET
(C618G +12 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+8 more
GPathogenic
RET
(C618S +12 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic
RET
(C620F +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GPathogenic
RET
(C634R +14 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GPathogenic/Likely pathogenic
RET
(K412N +13 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+8 more
GPathogenic/Likely pathogenic
RET
(G437S +16 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia
+9 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(intron variant)
not specified
+4 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GBenign
RET
(N783T +17 more)
Single nucleotide variant
(missense variant)
RET-related condition
+6 more
GConflicting classifications of pathogenicity
RET
(Y791F +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+9 more
GBenign/Likely benign
RET
(V804M +17 more)
Single nucleotide variant
(missense variant)
RET-related condition
+13 more
GPathogenic/Likely pathogenic
RET
(V804L +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia
+5 more
GPathogenic
RET
(Y806* +17 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
RET
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2
+8 more
GBenign/Likely benign
RET
(E843K +17 more)
Single nucleotide variant
(missense variant)
RET-related condition
+9 more
GConflicting classifications of pathogenicity
RET
(M608fs +1 more)
Deletion
(frameshift variant)
not provided
GPathogenic
RET
Single nucleotide variant
(intron variant)
not provided
+3 more
GBenign
RET
(V871I +17 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+9 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia
+9 more
GBenign
RET
(M918T +17 more)
Single nucleotide variant
(missense variant)
RET-related condition
+18 more
GPathogenic/Likely pathogenic
RET
(R982C +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+11 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia
+8 more
GConflicting classifications of pathogenicity
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