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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHFR, MSH3
Deletion
Familial adenomatous polyposis 4
+3 more
GBenign/Likely benign
MSH3
(N212H)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
MSH3
Single nucleotide variant
(splice acceptor variant)
not provided
+2 more
GUncertain significance
MSH3
(K738*)
Single nucleotide variant
(nonsense)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic/Likely pathogenic
MSH3
(I1082V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
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