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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MLH3
(A1394T +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
MLH3
(N1147I)
Single nucleotide variant
(missense variant)
Colorectal cancer, hereditary nonpolyposis, type 7
+4 more
GConflicting classifications of pathogenicity
MLH3
(G981S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MLH3
(S817G)
Single nucleotide variant
(missense variant)
not specified
+1 more
GLikely benign
MLH3
(Y238C)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
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