Transcript #00000027 (NM_000546.5, TP53 gene)

Transcript name transcript variant 1
Gene name TP53 (tumor protein p53)
Chromosome 17
Transcript - NCBI ID NM_000546.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_000537.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

74 entries on 1 page. Showing entries 1 - 74.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
./. 2i c.74+14T>C - r.(=) p.(=) - ClinVar
-?/. 3i c.97-28T>A - r.(=) p.(=) - ClinVar
+/. 4 c.337_339del - r.(?) p.(Phe113del) - -
+/. 4 c.370T>C - r.(?) p.(Cys124Arg) - -
+/. - c.380C>T - r.(?) p.(Ser127Phe) missense Likely pathogenic
./. 5 c.413C>T - r.(?) p.(Ala138Val) - ClinVar
?/. 5 c.454C>T - r.(?) p.(Pro152Ser) - ClinVar
+/. 5 c.455del - r.(?) p.(Pro152Argfs*18) - ClinVar
+/. 5 c.470T>G - r.(?) p.(Val157Gly) - -
+/. - c.472C>T - r.(?) p.(Arg158Cys) missense Likely pathogenic
+/. 5 c.488A>G - r.(?) p.(Tyr163Cys) - ClinVar
+/. 5 c.524G>A - r.(?) p.(Arg175His) - ClinVar
+/. 5 c.524G>A - r.(?) p.(Arg175His) - ClinVar
+?/. 5 c.527G>T - r.(?) p.(Cys176Phe) - ClinVar
./. 5 c.536A>G - r.(?) p.(His179Arg) - ClinVar
+/. 5 c.548C>G - r.(?) p.(Ser183*) - ClinVar
./. 6 c.578A>G - r.(?) p.(His193Arg) - ClinVar
+/. 6 c.586C>T - r.(?) p.(Arg196*) - ClinVar
+/. 6 c.586C>T - r.(?) p.(Arg196*) - ClinVar
+/. - c.586C>T - r.(?) p.(Arg196*) - Pathogenic
?/. 6 c.589G>T - r.(?) p.(Val197Leu) - ClinVar
?/. 6 c.589G>T - r.(?) p.(Val197Leu) - ClinVar
+/. 6 c.590_591delinsCC - r.(?) p.(Val197Ala) - -
+/. - c.596G>T - r.(?) p.(Gly199Val) - rs1555525857
+?/. 6 c.614A>G - r.(?) p.(Tyr205Cys) - ClinVar
./. 6 c.638G>C - r.(?) p.(Arg213Pro) - ClinVar
+/. 6 c.659A>G - r.(?) p.(Tyr220Cys) - ClinVar
+/. 6i c.672+18G>C - r.(=) p.(=) - ClinVar
+/. 7 c.683A>C - r.(?) p.(Asp228Ala) - -
+/. 7 c.683A>C - r.(?) p.(Asp228Ala) - -
+/. 7 c.693C>G - r.(=) p.(=) - -
+/. 7 c.693C>G - r.(=) p.(=) - -
+/. 7 c.700T>C - r.(?) p.(Tyr234His) - ClinVar
./. 7 c.701A>G - r.(?) p.(Tyr234Cys) - ClinVar
+/. 7 c.702C>G - r.(?) p.(Tyr234*) - -
+?/. 7 c.710T>A - r.(?) p.(Met237Lys) - ClinVar
+/. 7 c.711G>A - r.(?) p.(Met237Ile) - ClinVar
./. 7 c.731G>A - r.(?) p.(Gly244Asp) - ClinVar
+?/. 7 c.737T>A - r.(?) p.(Met246Lys) - ClinVar
+?/. 7 c.737T>A - r.(?) p.(Met246Lys) - ClinVar
+/. 7 c.742C>T - r.(?) p.(Arg248Trp) - ClinVar
+/. 7 c.742C>T - r.(?) p.(Arg248Trp) - ClinVar
+/. 7 c.743G>A - r.(?) p.(Arg248Gln) - ClinVar
?/. 7 c.746G>A - r.(?) p.(Arg249Lys) - ClinVar
?/. 7 c.746G>A - r.(?) p.(Arg249Lys) - ClinVar
+?/. - c.775G>T - r.(?) p.(Asp259Tyr) - ClinVar
+/. 8 c.793C>T - r.(=) p.(=) - -
+/. 8 c.794T>G - r.(?) p.(Leu265Arg) - -
+/. 8 c.794T>G - r.(?) p.(Leu265Arg) - -
+/. 8 c.798A>C - r.(=) p.(=) - -
+/. 8 c.798A>C - r.(=) p.(=) - -
+/. - c.800G>A - r.(?) p.(Arg267Gln) missense Uncertain significance​
./. 8 c.809T>C - r.(?) p.(Phe270Ser) - ClinVar
./. 8 c.817C>T - r.(?) p.(Arg273Cys) - ClinVar
+/. - c.817C>T - r.(?) p.(Arg273Cys) missense Pathogenic/Likely pathogenic
+/. 8 c.817_820del - r.(?) p.(Arg273Phefs*71) - -
+/. 8 c.831_857del - r.(?) p.(Cys277*) - -
./. 8 c.832C>T - r.(?) p.(Pro278Ser) - ClinVar
+/. 8 c.844C>G - r.(?) p.(Arg282Gly) - ClinVar
+/. - c.844C>T - r.(?) p.(Arg282Trp) - ClinVar
./. 8 c.844C>T - r.(?) p.(Arg282Trp) - ClinVar
./. 8 c.853G>A - r.(?) p.(Glu285Lys) - ClinVar
+/. 8 c.856G>A - r.(?) p.(Glu286Lys) - ClinVar
+/. 8 c.876del - r.(?) p.(Glu294Serfs*51) - -
./. 8 c.903A>G - r.(=) p.(=) - ClinVar
+/. - c.916C>T - r.(?) p.(Arg306*) - Pathogenic
+/. 8 c.916C>T - r.(?) p.(Arg306*) - ClinVar
+/. 9 c.960del - r.(?) p.(Lys321Asnfs*24) - -
+/. 10 c.1001_1006dup - r.(?) p.(Gly334_Arg335dup) - -
+/. 10 c.1006G>T - r.(?) p.(Glu336*) - -
+/. 10 c.1013_1014insT - r.(?) p.(Glu339Argfs*8) - -
+/. 10 c.1024C>T - r.(?) p.(Arg342*) - ClinVar
+/. 10 c.1036G>T - r.(?) p.(Glu346*) - ClinVar
+/. 4 c.*7657470C>G - r.(=) p.(=) - -
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