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Items: 23

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH3, DHFR
(S33G)
Single nucleotide variant
(5 prime UTR variant +2 more)
Familial adenomatous polyposis 4
+3 more
GUncertain significance
DHFR, MSH3
(S39T)
Single nucleotide variant
(5 prime UTR variant +2 more)
Familial adenomatous polyposis 4
+3 more
GUncertain significance
MSH3
(P96L)
Single nucleotide variant
(missense variant)
Endometrial carcinoma
+4 more
GUncertain significance
MSH3
(Q106E)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
MSH3
(S133C)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MSH3
(D357V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MSH3
(L421V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
MSH3
(E456K)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
MSH3
(Y465C)
Single nucleotide variant
(missense variant)
Endometrial carcinoma
+4 more
GUncertain significance
MSH3
(Y476H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
MSH3
(E512*)
Single nucleotide variant
(nonsense)
Endometrial carcinoma
+3 more
GPathogenic/Likely pathogenic
MSH3
(R574Q)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
MSH3
(R593Q)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
MSH3
(R669Q)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
MSH3
(I672V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MSH3
(P681S)
Single nucleotide variant
(missense variant)
MSH3-related condition
+4 more
GConflicting classifications of pathogenicity
MSH3
(P740S)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 4
+3 more
GUncertain significance
MSH3
(H827R)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
MSH3
(G896R)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
MSH3
(M899V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
MSH3
(I912S)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
MSH3
(R1061G)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MSH3
(H1114R)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 4
+2 more
GConflicting classifications of pathogenicity
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