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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTNNB1, LOC126806658
(D32G +1 more)
Single nucleotide variant
(missense variant)
Neoplasm of uterine cervix
+10 more
GPathogenic/Likely pathogenic
CTNNB1, LOC126806658
(S37C +1 more)
Single nucleotide variant
(missense variant)
Malignant neoplasm of body of uterus
+11 more
GPathogenic/Likely pathogenic
CTNNB1, LOC126806658
(T41A +1 more)
Single nucleotide variant
(missense variant)
Desmoid tumor
GLikely pathogenic
CTNNB1, LOC126806658
(S45P +1 more)
Single nucleotide variant
(missense variant)
Disease
+10 more
GPathogenic/Likely pathogenic
CTNNB1, LOC126806658
Single nucleotide variant
(synonymous variant)
not provided
GLikely pathogenic
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