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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MUTYH
(S515F +8 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GBenign/Likely benign
MUTYH
(E479K +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+2 more
GUncertain significance
MUTYH
(V329M +8 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
MUTYH
(Y165C +8 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+4 more
GPathogenic/Likely pathogenic
MUTYH
Single nucleotide variant
(synonymous variant +2 more)
not provided
+3 more
GConflicting classifications of pathogenicity
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