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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TP53
(E207K +3 more)
Single nucleotide variant
(missense variant +1 more)
TP53-related condition
+5 more
GConflicting classifications of pathogenicity
TP53
(R135Q +3 more)
Single nucleotide variant
(missense variant)
Li-Fraumeni syndrome
GUncertain significance
TP53
(R163C +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
TP53
(P43L +1 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
GLikely benign
TP53
(P8T)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
+2 more
GConflicting classifications of pathogenicity
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