Transcript #00023971 (NM_207037.1, TCF12 gene)

Transcript name transcript variant 2
Gene name TCF12 (transcription factor 12)
Chromosome 15
Transcript - NCBI ID NM_207037.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_996920.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2014-11-02 17:47:23 +01:00 (CET)
Date last edited N/A


Variants

89 entries on 1 page. Showing entries 1 - 89.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-23+8C>T r.(=) p.(=)
+?/. 2 c.-1G>A r.spl p.(=)
-/. - c.75+62_75+65del r.(=) p.(=)
+/. - c.86_87insGA r.(?) p.(Pro30AsnfsTer58)
-/. - c.135A>G r.(?) p.(Gln45=)
?/. - c.148+1G>A r.spl? p.?
?/. - c.268C>T r.(?) p.(Arg90Ter)
+/. - c.268C>T r.(?) p.(Arg90Ter)
-/. - c.297A>G r.(?) p.(Pro99=)
-?/. - c.311A>G r.(?) p.(Asn104Ser)
-?/. - c.311A>G r.(?) p.(Asn104Ser)
+?/. 6i_18i c.391-5871_1746-1795del r.? p.?
-?/. 7 c.454C>T r.(?) p.(Pro152Ser)
-?/. - c.530C>T r.(?) p.(Pro177Leu)
-/. - c.579+11A>G r.(=) p.(=)
-?/. - c.580-11935T>C r.(=) p.(=)
-?/. - c.580-11563C>T r.(=) p.(=)
-?/. - c.580-12T>C r.(=) p.(=)
+?/. 9 c.596dup r.(?) p.(Asn200Lysfs*4)
?/. - c.616C>T r.(?) p.(Arg206Cys)
?/. - c.616C>T r.(?) p.(Arg206Cys)
-?/. - c.685+10A>G r.(=) p.(=)
+/. - c.722C>G r.(?) p.(Ser241Ter)
+/. - c.778_779del r.(?) p.(Met260ValfsTer5)
+/. - c.825G>C r.(?) p.(Leu275Phe)
?/. - c.825+5G>T r.spl? p.?
-?/. - c.825+8A>G r.(=) p.(=)
-?/. - c.826-4C>A r.spl? p.?
+/. 10i c.826-2A>G r.spl p.?
+?/. 11 c.842C>G r.(?) p.(Ser281*)
+/. - c.842C>G r.(?) p.(Ser281Ter)
-/. - c.898G>A r.(?) p.(Gly300Ser)
-?/. - c.950A>G r.(?) p.(Asn317Ser)
-?/. - c.953G>A r.(?) p.(Gly318Glu)
+?/. - c.956C>A r.(?) p.(Ser319Ter)
+/. - c.970G>T r.(?) p.(Gly324Ter)
-?/. - c.970+203A>G r.(=) p.(=)
-?/. - c.971-3C>T r.spl? p.?
+?/. - c.1024G>C r.(?) p.(Ala342Pro)
?/. - c.1035+5G>C r.spl? p.?
?/. - c.1048G>A r.(?) p.(Asp350Asn)
?/. - c.1051C>G r.(?) p.(His351Asp)
+/. - c.1071del r.(?) p.(Ser358Glnfs*39)
-?/. - c.1071G>A r.(?) p.(Pro357=)
+/. - c.1073C>G r.(?) p.(Ser358Ter)
+/. - c.1115-2A>G r.spl? p.?
+/. - c.1123C>T r.(?) p.(Gln375Ter)
+?/. 14 c.1144C>T r.(?) p.(Gln382*)
+/. - c.1261-3C>G r.1260_1261insag p.Gln421Serfs*9
+?/. 16 c.1267C>T r.(?) p.(Arg423*)
-?/. - c.1303A>G r.(?) p.(Ile435Val)
+/. - c.1328dup r.(?) p.(Pro445ThrfsTer11)
+/. - c.1366dup r.(?) p.(Ile456AsnfsTer3)
+/. - c.1457C>A r.(?) p.(Ser486Ter)
+/. - c.1467+1G>A r.spl? p.?
-?/. - c.1474A>G r.(?) p.(Thr492Ala)
+/. - c.1491dup r.(?) p.(Val498Cysfs*12)
-?/. - c.1496G>C r.(?) p.(Ser499Thr)
-?/. - c.1508A>G r.(?) p.(Asn503Ser)
+/. - c.1514C>G r.(?) p.(Ser505Ter)
?/. 17 c.1520T>G r.(?) p.(Leu507Arg)
-?/. - c.1558C>G r.(?) p.(His520Asp)
+/. - c.1570G>T r.(?) p.(Glu524Ter)
+/. - c.1582+1G>T r.spl? p.?
-?/. - c.1582+7A>G r.(=) p.(=)
-?/. - c.1583-6T>C r.(=) p.(=)
+/. - c.1642_1645del r.(?) p.(Glu548Argfs*14)
+/. - c.1646del r.(?) p.(Lys549ArgfsTer14)
+/. - c.1713del r.(?) p.(Asp572IlefsTer19)
?/. - c.1745+3A>G r.spl? p.?
-?/. - c.1745+5T>C r.spl? p.?
+?/. 18i_19i c.1745+4562_1978+3153del r.? p.?
+?/. 18i_20i c.1746-1697_*11+65dup r.? p.?
-?/. - c.1746C>T r.(?) p.(Ser582=)
?/. - c.1807C>T r.(?) p.(Arg603Trp)
?/. - c.1831C>T r.(?) p.(Arg611Cys)
+?/. 19 c.1832G>A r.(?) p.(Arg611His)
?/. - c.1837C>T r.(?) p.(Arg613Cys)
+/. - c.1838G>A r.(?) p.(Arg613His)
?/. - c.1865A>G r.(?) p.(Lys622Arg)
+/. - c.1876C>T r.(?) p.(Arg626*)
-/. - c.1894T>C r.(?) p.(Leu632=)
+/. - c.1912C>G r.(?) p.(Gln638Glu)
?/. - c.1923_1925del r.(?) p.(Leu642del)
-?/. - c.1965A>G r.(?) p.(=)
?/. - c.1978+1G>A r.spl? p.?
+?/. 19i_20i c.1979-3147_*12-1497del r.? p.?
-?/. - c.1979-429C>G r.(=) p.(=)
-?/. - c.*12-4A>G r.spl? p.?
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