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Items: 1 to 100 of 873

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MUTYH
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MUTYH
Deletion
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MUTYH
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MUTYH
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MUTYH
(Q549* +7 more)
Single nucleotide variant
(nonsense +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
(A520fs +7 more)
Deletion
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
MUTYH
(A427T +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MUTYH
(S546R +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MUTYH
(N402I +12 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MUTYH
(H542Y +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MUTYH
(A541V +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+2 more
GUncertain significance
MUTYH
(A398fs +7 more)
Deletion
(frameshift variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
(D540N +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
MUTYH
(T539A +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MUTYH
(I537V +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
(H508Y +7 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
MUTYH
(R534Q +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GBenign/Likely benign
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Familial adenomatous polyposis 2
+1 more
GLikely benign
MUTYH
(R534W +7 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GUncertain significance
MUTYH
(F533L +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MUTYH
(F532L +7 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
MUTYH
(N388del +7 more)
Deletion
(inframe_deletion +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Familial adenomatous polyposis 2
+2 more
GLikely benign
MUTYH
(D530H +8 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+2 more
GUncertain significance
MUTYH
(D530Y +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
MUTYH
(L529M +8 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GBenign/Likely benign
MUTYH
(M381I +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MUTYH
(M381I +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
(M524L +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
(M524V +7 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity
MUTYH
(M524L +8 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
MUTYH
(R523H +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
MUTYH
(R523C +7 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
MUTYH
(P522L +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MUTYH
(P509S +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
(R519Q +8 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GLikely benign
MUTYH
(R519W +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Familial adenomatous polyposis 2
+4 more
GConflicting classifications of pathogenicity
MUTYH
(P516L +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+3 more
GConflicting classifications of pathogenicity
MUTYH
(P516T +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
(S515F +8 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+3 more
GBenign/Likely benign
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GBenign/Likely benign
MUTYH
(V393E +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MUTYH
(V513M +7 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
MUTYH
(V513L +8 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
(Q369E +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
(S511F +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Familial adenomatous polyposis 2
+2 more
GLikely benign
MUTYH
(K366E +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MUTYH
Single nucleotide variant
(intron variant)
Familial adenomatous polyposis 2
+2 more
GLikely benign
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MUTYH
Single nucleotide variant
(intron variant)
Familial adenomatous polyposis 2
+1 more
GLikely benign
MUTYH
Deletion
(intron variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MUTYH
Single nucleotide variant
(intron variant)
not specified
+2 more
GLikely benign
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GLikely benign
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MUTYH
Single nucleotide variant
(intron variant)
Familial adenomatous polyposis 2
+1 more
GConflicting classifications of pathogenicity
MUTYH
Single nucleotide variant
(splice donor variant)
Hereditary cancer-predisposing syndrome
GLikely pathogenic
MUTYH
Single nucleotide variant
(splice donor variant)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic/Likely pathogenic
MUTYH
(C505Y +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+2 more
GUncertain significance
MUTYH
(C505G +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+2 more
GUncertain significance
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Familial adenomatous polyposis 2
+1 more
GLikely benign
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Familial adenomatous polyposis 2
+1 more
GLikely benign
MUTYH
(G503E +8 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+6 more
GConflicting classifications of pathogenicity
MUTYH
(G503W +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MUTYH
(Q498R +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MUTYH
(Q501* +7 more)
Single nucleotide variant
(nonsense +1 more)
Familial adenomatous polyposis 2
+3 more
GConflicting classifications of pathogenicity
MUTYH
(G499S +7 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GUncertain significance
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MUTYH
(Q495H +8 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MUTYH
(Q498R +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
MUTYH
Indel
(inframe_indel +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MUTYH
(V353A +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
(R495H +8 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
MUTYH
(R495C +7 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GUncertain significance
MUTYH
(F351L +7 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
MUTYH
(V493F +8 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GPathogenic/Likely pathogenic
MUTYH
(V493I +7 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GLikely benign
MUTYH
Microsatellite
(intron variant)
Familial adenomatous polyposis 2
+3 more
GLikely benign
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+3 more
GLikely benign
MUTYH
Single nucleotide variant
(intron variant)
Familial adenomatous polyposis 2
+1 more
GLikely benign
MUTYH
Deletion
(intron variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MUTYH
Microsatellite
(intron variant)
Hereditary cancer-predisposing syndrome
GLikely benign
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MUTYH
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MUTYH
Single nucleotide variant
(intron variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MUTYH
Single nucleotide variant
(intron variant)
Familial adenomatous polyposis 2
+1 more
GUncertain significance
MUTYH
Deletion
(splice donor variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely pathogenic
MUTYH
Single nucleotide variant
(splice donor variant)
Familial adenomatous polyposis 2
+3 more
GConflicting classifications of pathogenicity
MUTYH
(K492* +7 more)
Single nucleotide variant
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic/Likely pathogenic
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