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Items: 1 to 100 of 647

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GBenign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
TP53
(D261N +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
+2 more
GConflicting classifications of pathogenicity
TP53
(D391E +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
TP53
(E256A +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
GLikely benign
TP53
(M252T +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
(M252V +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
Single nucleotide variant
(synonymous variant +1 more)
Li-Fraumeni syndrome
+4 more
GBenign/Likely benign
TP53
Single nucleotide variant
(synonymous variant +1 more)
Li-Fraumeni syndrome
+1 more
GConflicting classifications of pathogenicity
TP53
(R247H +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
(R247L +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
(R247S +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
(R247C +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
TP53
(S244F +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
TP53
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
TP53
(G242R +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
GLikely benign
TP53
(G242S +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
TP53
(K334N +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
+1 more
GUncertain significance
TP53
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
TP53
(K334R +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
+2 more
GConflicting classifications of pathogenicity
TP53
(K240R +3 more)
Single nucleotide variant
(missense variant +1 more)
TP53-related disorder
+2 more
GConflicting classifications of pathogenicity
TP53
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
(H329N +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
+2 more
GUncertain significance
TP53
(H236Y +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
Single nucleotide variant
(intron variant)
Li-Fraumeni syndrome
+2 more
GConflicting classifications of pathogenicity
TP53
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
TP53
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
TP53
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
TP53
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
TP53
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
TP53
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
TP53
(S234C +3 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
TP53
(S234A +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
GLikely benign
TP53
Single nucleotide variant
(synonymous variant +1 more)
Li-Fraumeni syndrome
+1 more
GLikely benign
TP53
(H233Y +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
GLikely benign
TP53
(A364V +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
+2 more
GUncertain significance
TP53
(G361R +3 more)
Single nucleotide variant
(missense variant +1 more)
Adrenocortical carcinoma, hereditary
+3 more
GUncertain significance
TP53
(G228V +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
+3 more
GConflicting classifications of pathogenicity
TP53
(G228A +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
GLikely benign
TP53
(G228R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GConflicting classifications of pathogenicity
TP53
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
(P200R +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
TP53
(E226V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity
TP53
(G197R +3 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
GConflicting classifications of pathogenicity
TP53
(G224R +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
(A196D +3 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
TP53
(A355V +3 more)
Single nucleotide variant
(missense variant +1 more)
Adrenocortical carcinoma, hereditary
+3 more
GConflicting classifications of pathogenicity
TP53
Single nucleotide variant
(synonymous variant +1 more)
Li-Fraumeni syndrome
+2 more
GLikely benign
TP53
(Q354R +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
+2 more
GUncertain significance
TP53
(Q222K +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
(L191V +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
+2 more
GConflicting classifications of pathogenicity
TP53
(E184fs +3 more)
Deletion
(frameshift variant +1 more)
Li-Fraumeni syndrome
+1 more
GPathogenic/Likely pathogenic
TP53
(R210Q +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
(R210* +3 more)
Single nucleotide variant
(nonsense +1 more)
Adrenocortical carcinoma, hereditary
+14 more
GPathogenic
TP53
Single nucleotide variant
(synonymous variant +1 more)
Li-Fraumeni syndrome 1
+3 more
GBenign/Likely benign
TP53
(E207K +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
+5 more
GConflicting classifications of pathogenicity
TP53
(E207Q +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
GLikely benign
TP53
(F206L +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
TP53
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+5 more
GBenign/Likely benign
TP53
(F206C +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
TP53
(R205P +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
+2 more
GLikely pathogenic
TP53
(R337H +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+17 more
GPathogenic/Likely pathogenic
TP53
(R205C +3 more)
Single nucleotide variant
(missense variant +1 more)
Adrenocortical carcinoma, hereditary
+4 more
GPathogenic/Likely pathogenic
TP53
(R296H +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
TP53
(R203C +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome
GUncertain significance
TP53
(G202W +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
+1 more
GLikely pathogenic
TP53
(R201H +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
(R201C +3 more)
Single nucleotide variant
(missense variant +1 more)
Li-Fraumeni syndrome 1
GLikely benign
TP53
Single nucleotide variant
(synonymous variant +1 more)
Li-Fraumeni syndrome 1
+3 more
GLikely benign
TP53
Single nucleotide variant
(intron variant)
Li-Fraumeni syndrome 1
+2 more
GLikely benign
TP53
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign/Likely benign
TP53
Deletion
(intron variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GBenign/Likely benign
TP53
Insertion
(intron variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Duplication
(frameshift variant +3 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
TP53
Single nucleotide variant
(synonymous variant +2 more)
Li-Fraumeni syndrome 1
+2 more
GLikely benign
TP53
(S214L +3 more)
Single nucleotide variant
(missense variant +2 more)
Li-Fraumeni syndrome 1
+3 more
GLikely benign
TP53
Single nucleotide variant
(synonymous variant +2 more)
Hereditary cancer-predisposing syndrome
GLikely benign
TP53
Single nucleotide variant
(synonymous variant +2 more)
Li-Fraumeni syndrome 1
+4 more
GLikely benign
TP53
(S213L +3 more)
Single nucleotide variant
(missense variant +2 more)
not specified
+1 more
GConflicting classifications of pathogenicity
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