Transcript #00020854 (NM_016569.3, TBX3 gene)

Transcript name transcript variant 2
Gene name TBX3 (T-box 3)
Chromosome 12
Transcript - NCBI ID NM_016569.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_057653.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

64 entries on 1 page. Showing entries 1 - 64.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-727T>C r.(=) p.(=)
-/. - c.-727T>C r.(=) p.(=)
-/. - c.-29G>T r.(?) p.(=)
-?/. - c.11C>T r.(?) p.(Ser4Phe)
?/. - c.14dup r.(?) p.(Met5Ilefs*106)
-/. - c.61C>T r.(?) p.(=)
-?/. - c.66T>C r.(?) p.(Pro22=)
-?/. - c.97G>T r.(?) p.(Val33Leu)
?/. - c.182C>A r.(?) p.(Ala61Asp)
?/. - c.277A>G r.(?) p.(Met93Val)
-?/. - c.281A>G r.(?) p.(Glu94Gly)
?/. - c.370G>A r.(?) p.(Val124Ile)
-?/. - c.390-4A>G r.spl? p.?
+/. - c.586C>T r.(?) p.(Gln196Ter)
-?/. - c.619C>T r.(?) p.(=)
+?/. - c.718-2A>G r.spl? p.?
-?/. - c.760A>G r.(?) p.(Ile254Val)
-?/. - c.795T>C r.(?) p.(=)
?/. - c.820C>T r.(?) p.(Pro274Ser)
-/. - c.837C>T r.(?) p.(Ile279=)
-?/. - c.837C>T r.(?) p.(Ile279=)
?/. - c.889A>C r.(?) p.(Asn297His)
+/. - c.928C>T r.(?) p.(Arg310Ter)
+/. - c.946C>T r.(?) p.(Gln316Ter)
?/. - c.968G>A r.(?) p.(Arg323Lys)
+/. - c.992del r.(?) p.(Lys331ArgfsTer30)
+/. - c.1099+2T>C r.spl? p.?
-/. - c.1154A>G r.(?) p.(His385Arg)
-?/. - c.1154A>G r.(?) p.(His385Arg)
?/. - c.1175C>T r.(?) p.(Ala392Val)
-/. - c.1186T>A r.(?) p.(Ser396Thr)
-/. - c.1186T>A r.(?) p.(Ser396Thr)
-/. - c.1186T>A r.(?) p.(Ser396Thr)
-?/. - c.1233G>C r.(?) p.(Ala411=)
-/. - c.1233G>C r.(?) p.(Ala411=)
?/. - c.1279C>T r.(?) p.(Arg427Trp)
?/. - c.1292C>T r.(?) p.(Ala431Val)
-/. - c.1296G>T r.(?) p.(Ser432=)
-?/. - c.1310A>G r.(?) p.(His437Arg)
?/. - c.1370C>G r.(?) p.(Pro457Arg)
-?/. - c.1378G>A r.(?) p.(Glu460Lys)
?/. - c.1385C>G r.(?) p.(Thr462Arg)
?/. - c.1454A>G r.(?) p.(Gln485Arg)
?/. - c.1514C>T r.(?) p.(Pro505Leu)
-/. - c.1522G>A r.(?) p.(Ala508Thr)
-?/. - c.1544G>A r.(?) p.(Gly515Glu)
-?/. - c.1600A>G r.(?) p.(Met534Val)
-?/. - c.1685C>T r.(?) p.(Ala562Val)
+/. - c.1770+1G>A r.spl? p.?
-?/. - c.1791C>G r.(?) p.(Phe597Leu)
?/. - c.1817C>T r.(?) p.(Thr606Met)
-?/. - c.1818G>T r.(?) p.(Thr606=)
?/. - c.1822A>G r.(?) p.(Met608Val)
-?/. - c.1832C>A r.(?) p.(Ala611Glu)
?/. - c.1837G>C r.(?) p.(Ala613Pro)
-?/. - c.1843T>G r.(?) p.(Ser615Ala)
-?/. - c.1891C>A r.(?) p.(Leu631Met)
?/. - c.1913T>A r.(?) p.(Leu638Gln)
-?/. - c.1950G>A r.(?) p.(Pro650=)
-?/. - c.2078A>G r.(?) p.(Asn693Ser)
-?/. - c.2105G>A r.(?) p.(Ser702Asn)
?/. - c.2213C>T r.(?) p.(Ser738Phe)
-?/. - c.2221G>C r.(?) p.(Ala741Pro)
-?/. - c.2222C>T r.(?) p.(Ala741Val)
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