Transcript #00025349 (NM_001114979.1, TP63 gene)

Transcript name transcript variant 3
Gene name TP63 (tumor protein p63)
Chromosome 3
Transcript - NCBI ID NM_001114979.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001108451.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2018-12-14 16:38:22 +01:00 (CET)
Date last edited N/A


Variants

130 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     
./. - c.-58A>T r.(=) p.(=) -
+/. _1_14_ ACMG: 5 r.0 p.0 -
-?/. - c.19C>T r.(?) p.(Arg7Trp) -
-/. - c.191+24T>C r.(=) p.(=) -
-/. - c.191+24T>C r.(=) p.(=) -
-/. - c.191+24T>C r.(=) p.(=) -
./. - c.191+24T>C r.(=) p.(=) -
?/. - c.284G>A r.(?) p.(Cys95Tyr) -
-/. - c.325-18546_325-18543dup r.(=) p.(=) -
-/. - c.325-18543_325-18542insAG r.(=) p.(=) -
-/. - c.325-18543_325-18542insAG r.(=) p.(=) -
-/. - c.325-18543_325-18542insAGAG r.(=) p.(=) -
+/. - c.325-18441C>T r.(=) p.(=) -
-/. - c.325-76C>A r.(=) p.(=) -
./. - c.325-34C>T r.(=) p.(=) -
?/. - c.325-7C>T r.(=) p.(=) -
+/. - c.343G>T r.(?) p.(Gly115Trp) -
?/. - c.416C>T r.(?) p.(Ala139Val) -
+/. - c.518G>T r.(?) p.(Gly173Val) -
./. - c.518G>T r.(?) p.(Gly173Val) -
./. - c.579+39T>A r.(=) p.(=) -
./. - c.579+92C>T r.(=) p.(=) -
-/. - c.580-20047del r.(=) p.(=) -
./. - c.580-2A>G r.spl? p.? -
+?/. - c.604T>C r.(?) p.(Tyr202His) -
+?/. - c.619A>G r.(?) p.(Lys207Glu) -
./. - c.678C>T r.(=) p.(=) -
+?/. - c.691T>C r.(?) p.(Tyr231His) -
+/. - c.692A>G r.(?) p.(Tyr231Cys) -
+/. - c.692A>G r.(?) p.(Tyr231Cys) -
-?/. - c.699A>G r.(?) p.(Lys233=) -
+/. - c.721G>A r.(?) p.(Val241Met) -
+/. - c.727C>T r.(?) p.(Arg243Trp) -
+/. - c.727C>T r.(?) p.(Arg243Trp) -
+/. - c.728G>A r.(?) p.(Arg243Gln) -
+/. - c.728G>A r.(?) p.(Arg243Gln) -
+/. - c.739C>T r.(?) p.(His247Tyr) -
+?/. - c.740A>C r.(?) p.(His247Pro) -
./. - c.766+34T>G r.(=) p.(=) -
./. - c.766+42G>A r.(=) p.(=) -
./. - c.767-35A>G r.(=) p.(=) -
+/. - c.796C>T r.(?) p.(Arg266*) -
+/. - c.797G>A r.(?) p.(Arg266Gln) -
+/. - c.797G>A r.(?) p.(Arg266Gln) -
-?/. - c.799G>A r.(?) p.(Val267Ile) -
-/. - c.859C>T r.(?) p.(Leu287=) -
./. - c.859C>T r.(=) p.(=) -
?/. - c.866C>A r.(?) p.(Pro289His) -
?/. - c.881A>G r.(?) p.(Gln294Arg) -
./. - c.882+68G>A r.(=) p.(=) -
-/. - c.883-139A>G r.(=) p.(=) -
./. - c.912C>T r.(=) p.(=) -
-?/. - c.918C>T r.(?) p.(Phe306=) -
+/. - c.923G>A r.(?) p.(Cys308Tyr) -
+?/. - c.926A>G r.(?) p.(Asn309Ser) -
+?/. - c.929G>A r.(?) p.(Ser310Asn) -
+?/. - c.943G>T r.(?) p.(Gly315Trp) -
+?/. - c.943G>T r.(?) p.(Gly315Trp) -
+/. - c.952C>T r.(?) p.(Arg318Cys) -
+/. - c.952C>T r.(?) p.(Arg318Cys) -
+/. - c.953G>A r.(?) p.(Arg318His) -
+/. - c.955C>T r.(?) p.(Arg319Cys) -
+/. - c.956G>A r.(?) p.(Arg319His) -
+/. - c.1010G>A r.(?) p.(Arg337Gln) -
./. - c.1010G>A r.(?) p.(Arg337Gln) -
+?/. - c.1013G>A r.(?) p.(Arg338His) -
+/. - c.1027C>T r.(?) p.(Arg343Trp) -
+/. - c.1027C>T r.(?) p.(Arg343Trp) -
+/. - c.1028G>A r.(?) p.(Arg343Gln) -
+/. - c.1028G>A r.(?) p.(Arg343Gln) -
+/. - c.1033T>C r.(?) p.(Cys345Arg) -
+?/. - c.1034G>T r.(?) p.(Cys345Phe) -
+/. - c.1040G>A r.(?) p.(Cys347Tyr) -
+/. - c.1042C>G r.(?) p.(Pro348Ala) -
+/. - c.1042C>T r.(?) p.(Pro348Ser) -
+?/. - c.1061C>A r.(?) p.(Ala354Glu) -
./. - c.1062G>A r.(=) p.(=) -
-?/. - c.1121C>T r.(?) p.(Thr374Met) -
./. - c.1129+45C>T r.(=) p.(=) -
./. - c.1130-22A>G r.(=) p.(=) -
?/. - c.1178G>A r.(?) p.(Arg393Gln) -
./. - c.1212+43T>C r.(=) p.(=) -
-/. - c.1212+79A>G r.(=) p.(=) -
./. - c.1212+79A>G r.(=) p.(=) -
-?/. - c.1213-4A>G r.spl? p.? -
-?/. - c.1325A>G r.(?) p.(Gln442Arg) -
?/. - c.1339C>T r.(?) p.(Leu447Phe) -
-/. - c.1349+40G>C r.(=) p.(=) -
./. - c.1349+40G>C r.(=) p.(=) -
./. - c.1349+41G>A r.(=) p.(=) -
./. - c.1349+66G>A r.(=) p.(=) -
?/. 15 c.1390C>T r.(?) p.(Arg464Trp) -
-?/. - c.1405A>G r.(?) p.(Lys469Glu) -
-/. - c.*6182T>G r.(=) p.(=) -
./. - c.*6182T>G r.(=) p.(=) -
-/. - c.*6193T>C r.(=) p.(=) -
./. - c.*6193T>C r.(=) p.(=) -
?/. - c.*6293C>T r.(=) p.(=) -
?/. - c.*6368C>A r.(=) p.(=) -
-?/. - c.*9159C>T r.(=) p.(=) -
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