Transcript #00025260 (NM_005650.2, TCF20 gene)

Transcript name transcript variant 1
Gene name TCF20 (transcription factor 20 (AR1))
Chromosome 22
Transcript - NCBI ID NM_005650.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_005641.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2018-03-22 08:58:05 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-17288G>A r.(?) p.(=)
+/. - c.(-36-23351_-36-23350)inv r.? p.?
?/. - c.7T>C r.(?) p.(Ser3Pro)
?/. - c.13C>G r.(?) p.(Arg5Gly)
-?/. - c.47G>C r.(?) p.(Ser16Thr)
./. - c.47G>C r.(?) p.(Ser16Thr)
./. - c.47G>C r.(?) p.(Ser16Thr)
?/. - c.74C>G r.(?) p.(Ser25Cys)
?/. - c.74C>T r.(?) p.(Ser25Phe)
?/. - c.101A>G r.(?) p.(Gln34Arg)
-/. - c.138C>T r.(?) p.(=)
./. - c.162_167del r.(?) p.(Ser55_Gly56del)
./. - c.162_167del r.(?) p.(Ser55_Gly56del)
-?/. - c.191C>T r.(?) p.(Ala64Val)
?/. - c.221C>G r.(?) p.(Ser74Cys)
-?/. - c.227A>C r.(?) p.(His76Pro)
?/. - c.239A>G r.(?) p.(Gln80Arg)
-?/. - c.295G>A r.(?) p.(Val99Met)
+?/. 2 c.313C>T r.(?) p.(Gln105*)
+?/. - c.385C>T r.(?) p.(Gln129Ter)
?/. - c.395G>A r.(?) p.(Ser132Asn)
-?/. - c.519C>T r.(?) p.(Ser173=)
+?/. - c.520C>T r.(?) p.(Gln174*)
-?/. - c.534_536dup r.(?) p.(Gln179dup)
?/. - c.647C>T r.(?) p.(Thr216Ile)
-?/. - c.702C>G r.(?) p.(His234Gln)
-?/. - c.737_739del r.(?) p.(Ser246del)
-?/. - c.737_739dup r.(?) p.(Ser246dup)
?/. - c.754C>T r.(?) p.(Arg252Cys)
-?/. - c.755G>A r.(?) p.(Arg252His)
?/. - c.796G>C r.(?) p.(Val266Leu)
+/. - c.904C>T r.(?) p.(Gln302*)
?/. - c.948_950dup r.(?) p.(Gln317dup)
+?/. - c.951del r.(?) p.(Gln317Hisfs*12)
+?/. - c.955C>T r.(?) p.(Gln319*)
+/. - c.964dup r.(?) p.(Gln322ProfsTer12)
./. - c.966_968del r.(?) p.(Gln322del)
./. - c.966_968del r.(?) p.(Gln322del)
-?/. - c.966_968del r.(?) p.(Gln322del)
+/. - c.993T>A r.(?) p.(Tyr331Ter)
?/. - c.997A>G r.(?) p.(Asn333Asp)
-?/. - c.1056T>C r.(?) p.(Val352=)
+?/. - c.1132C>T r.(?) p.(Gln378Ter)
-?/. - c.1186C>A r.(?) p.(Leu396Ile)
?/. - c.1289C>G r.(?) p.(Ser430Cys)
-?/. - c.1434C>T r.(?) p.(=)
-/. - c.1440T>G r.(?) p.(=)
+?/. - c.1462dup r.(?) p.(Arg488Lysfs*10)
?/. - c.1481_1487del r.(?) p.(Lys494IlefsTer16)
./. - c.1534A>G r.(?) p.(Lys512Glu)
-?/. - c.1549G>C r.(?) p.(Glu517Gln)
+?/. - c.1594G>T r.(?) p.(Glu532*)
+?/. - c.1623dup r.(?) p.(Thr542HisfsTer4)
-?/. - c.1715A>G r.(?) p.(Asn572Ser)
?/. - c.1723C>T r.(?) p.(Pro575Ser)
-?/. - c.1781A>G r.(?) p.(Asp594Gly)
-?/. - c.1799A>G r.(?) p.(Asn600Ser)
?/. - c.1810G>C r.(?) p.(Val604Leu)
?/. - c.1856A>G r.(?) p.(Lys619Arg)
-?/. - c.1926_1928del r.(?) p.(Gly643del)
?/. - c.1955T>G r.(?) p.(Leu652Arg)
-?/. - c.2120A>G r.(?) p.(Tyr707Cys)
?/. - c.2177A>G r.(?) p.(Gln726Arg)
?/. - c.2189G>A r.(?) p.(Gly730Glu)
+?/. - c.2221del r.(?) p.(Glu741Asnfs*42)
+?/. - c.2224C>T r.(?) p.(Arg742Ter)
-?/. - c.2335G>A r.(?) p.(Ala779Thr)
+?/. - c.2415dup r.(?) p.(Lys806Glnfs*25)
+?/. - c.2497C>T r.(?) p.(Gln833Ter)
+?/. - c.2712_2713del r.(?) p.(Gln906Valfs*28)
-?/. - c.2835G>C r.(?) p.(Lys945Asn)
-?/. - c.2885G>A r.(?) p.(Arg962His)
?/. - c.2891A>G r.(?) p.(Asn964Ser)
-?/. - c.2957C>T r.(?) p.(Thr986Met)
?/. - c.2968C>T r.(?) p.(Arg990Trp)
-?/. - c.2993G>A r.(?) p.(Arg998Gln)
-?/. - c.3072A>G r.(?) p.(Arg1024=)
?/. - c.3097A>G r.(?) p.(Met1033Val)
-?/. - c.3151C>T r.(?) p.(Pro1051Ser)
+/. - c.3207dup r.(?) p.(His1070SerfsTer7)
?/. - c.3209A>G r.(?) p.(His1070Arg)
?/. - c.3286G>A r.(?) p.(Glu1096Lys)
-?/. - c.3307G>A r.(?) p.(Gly1103Ser)
-?/. - c.3397C>T r.(?) p.(Arg1133Trp)
-?/. - c.3398G>A r.(?) p.(Arg1133Gln)
+/. - c.3423_3426dup r.(?) p.(Met1143TrpfsTer13)
?/. - c.3442C>T r.(?) p.(Pro1148Ser)
+?/. 2 c.3456C>A r.(?) p.(Tyr1152*)
-?/. - c.3495G>A r.(?) p.(Met1165Ile)
./. - c.3495G>A r.(?) p.(Met1165Ile)
-?/. - c.3496T>C r.(?) p.(Ser1166Pro)
./. - c.3518del r.(?) p.(Lys1173Argfs*5)
-?/. - c.3562T>C r.(?) p.(Cys1188Arg)
-?/. - c.3604G>A r.(?) p.(Gly1202Ser)
-?/. - c.3701G>C r.(?) p.(Ser1234Thr)
./. - c.3837del r.(?) p.(Asp1280Ilefs*71)
-?/. - c.3848G>A r.(?) p.(Arg1283His)
?/. - c.3853C>T r.(?) p.(Leu1285Phe)
?/. - c.3854T>A r.(?) p.(Leu1285His)
?/. - c.3860C>G r.(?) p.(Ser1287Ter)
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