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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AXIN2
(P740S +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+2 more
GUncertain significance
AXIN2
(A643P +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+2 more
GConflicting classifications of pathogenicity
AXIN2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
AXIN2
(F570V)
Single nucleotide variant
(missense variant)
Carcinoma of colon
+4 more
GUncertain significance
AXIN2
(S479Y)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
AXIN2
(P455A)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+2 more
GUncertain significance
AXIN2
(S376W)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
AXIN2
(L333P)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(S300fs)
Deletion
(frameshift variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(S244L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
AXIN2
(R68Q)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+3 more
GConflicting classifications of pathogenicity
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