Transcript #00026061 (NM_001953.4, TYMP gene)

Transcript name transcript variant 2
Gene name TYMP (thymidine phosphorylase)
Chromosome 22
Transcript - NCBI ID NM_001953.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_001944.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2026-03-04 16:53:42 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.*36C>T r.(?) p.(=)
+/. - c.-698464_*3781255del r.0? p.0?
-?/. - c.-10-36G>T r.spl p.(=)
+/. 1i c.-10-1G>C r.-11_417del p.0?
+/. 1i c.-10-1G>C r.spl p.?
+/. 2 c.? r.? p.?
+?/. - c.11del r.(?) p.(Leu4Ter)
-?/. - c.30G>A r.(?) p.(Gly10=)
?/. - c.47G>C r.(?) p.(Gly16Ala)
-?/. - c.61G>C r.(?) p.(Glu21Gln)
+/. - c.130C>T r.(?) p.(Arg44Ter)
+/. 2 c.131G>A r.(?) p.(Arg44Gln)
-?/. - c.194G>A r.(?) p.(Ser65Asn)
-/. - c.204C>T r.(?) p.(Gly68=)
+/. - c.214+1G>T r.spl p.?
-?/. - c.214+13G>A r.(=) p.(=)
?/. - c.214+17G>A r.(=) p.(=)
+/. 2i c.215-1G>C r.184_417del p.Asn63_Val140del
+/. - c.215-1G>C r.spl p.?
+/. - c.215-1G>C r.spl p.?
+/. - c.235C>T r.(?) p.(Arg79Ter)
?/. - c.242G>A r.(?) p.(Arg81Gln)
-?/. - c.242G>A r.(?) p.(Arg81Gln)
-?/. - c.242G>A r.(?) p.(Arg81Gln)
-?/. - c.294G>A r.(?) p.(Ser98=)
+?/. - c.342C>G r.(?) p.(Asp114Glu)
?/. - c.345G>T r.(?) p.(Lys115Asn)
+?/. - c.355G>A r.(?) p.(Gly119Arg)
+?/. - c.355G>A r.(?) p.(Gly119Arg)
+?/. - c.391C>A r.(?) p.(Pro131Thr)
+/. 4 c.433G>A r.(?) p.(Gly145Arg)
+/. 4 c.433G>A r.(?) p.(Gly145Arg)
+/. 4 c.433G>A r.(?) p.(Gly145Arg)
+/. 4 c.433G>A r.(?) p.(Gly145Arg)
?/. - c.437G>A r.(?) p.(Arg146His)
+/. - c.457G>A r.(?) p.(Gly153Ser)
+/. 4 c.457G>A r.(?) p.(Gly153Ser)
+/. 4 c.457G>A r.(?) p.(Gly153Ser)
+/. 4 c.457G>A r.(?) p.(Gly153Ser)
+/. - c.457G>A r.(?) p.(Gly153Ser)
+/. 4i c.478T>C r.(?) p.(Ser160Pro)
-?/. - c.494A>G r.(?) p.(Asn165Ser)
-?/. - c.495T>C r.(?) p.(Asn165=)
+/. - c.516+2T>A r.spl p.?
+/. 4i c.516+2T>C r.418_516del p.Val140_Gln172del
-?/. - c.516+16G>A r.(=) p.(=)
+/. 5 c.518T>G r.(?) p.(Met173Arg)
-?/. - c.519G>A r.(?) p.(Met173Ile)
?/. - c.542G>A r.(?) p.(Gly181Asp)
?/. - c.554T>A r.(?) p.(Val185Glu)
+/. - c.605G>C r.(?) p.(Arg202Thr)
+/. - c.622G>A r.(?) p.(Val208Met)
+/. - c.622G>A r.(?) p.(Val208Met)
+/. - c.622G>A r.(?) p.(Val208Met)
+/. - c.622G>A r.(?) p.(Val208Met)
+/. 6 c.653T>G r.(?) p.(Ile218Ser)
+/. 6 c.665A>G r.(?) p.(Lys222Arg)
-?/. - c.676G>A r.(?) p.(Gly226Arg)
-?/. - c.676G>A r.(?) p.(Gly226Arg)
?/. - c.685G>C r.(?) p.(Ala229Pro)
-?/. - c.735G>A r.(?) p.(Gln245=)
?/. - c.736G>A r.(?) p.(Glu246Lys)
-?/. - c.762G>A r.(?) p.(Thr254=)
+?/. - c.798_801dup r.(?) p.(Ala268ArgfsTer?)
-?/. - c.831G>A r.(?) p.(Leu277=)
+/. - c.854T>C r.(?) p.(Leu285Pro)
+/. 7i c.865G>A r.(?) p.(Glu289Lys)
+/. - c.866A>C r.(?) p.(Glu289Ala)
+/. 7 c.866A>C r.(?) p.(Glu289Ala)
+/. 7 c.866A>G r.(?) p.(Glu289Gly)
+/. 7 c.866A>G r.(?) p.(Glu289Gly)
+/. 7 c.866A>G r.(?) p.(Glu289Gly)
+/. 7 c.866A>G r.(?) p.(Glu289Gly)
+/. 7 c.866A>G r.(?) p.(Glu289Gly)
+/. 7 c.866A>G r.(?) p.(Glu289Gly)
+?/. - c.895C>A r.(?) p.(Pro299Thr)
-?/. - c.928+10dup r.(=) p.(=)
-?/. - c.929-6_929-3del r.spl? p.?
+?/. 7i c.929-6_929-3del r.spl p.?
+?/. - c.929-1G>A r.spl p.?
?/. - c.929G>A r.(?) p.(Gly310Glu)
+/. - c.931G>C r.(?) p.(Gly311Arg)
+/. - c.945G>A r.(?) p.(Trp315Ter)
-/. - c.972C>T r.(?) p.(Ala324=)
-/. - c.972C>T r.(?) p.(Ala324=)
-?/. - c.975G>A r.(?) p.(Gln325=)
+/. - c.1013C>A r.(?) p.(Ser338Ter)
+/. - c.1048C>T r.(?) p.(Gln350Ter)
-?/. - c.1074A>G r.(?) p.(Arg358=)
?/. - c.1103G>A r.(?) p.(Arg368His)
?/. - c.1109A>G r.(?) p.(Gln370Arg)
?/. - c.1138_1140del r.(?) p.(Glu380del)
?/. - c.1159G>A r.(?) p.(Gly387Ser)
-?/. - c.1159+18C>A r.(=) p.(=)
-?/. - c.1160-29C>G r.(=) p.(=)
-?/. - c.1160-26G>A r.(=) p.(=)
+/. 8i c.1160-1G>A r.1160_1300del p.Thr388_Gly434del
+/. 8i c.1160-1G>A r.1160_1300del p.Thr388_Gly434del
+/. - c.1160-1G>A r.spl p.?
+/. 8i c.1160-1G>A r.1160_1300del p.Thr388_Gly434del
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