Transcript #00021872 (NM_004239.3, TRIP11 gene)

Transcript name thyroid hormone receptor interactor 11
Gene name TRIP11 (thyroid hormone receptor interactor 11)
Chromosome 14
Transcript - NCBI ID NM_004239.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_004230.2
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

78 entries on 1 page. Showing entries 1 - 78.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.88A>G r.(?) p.(Ile30Val)
-?/. - c.140-4G>A r.spl? p.?
?/. - c.168A>T r.(?) p.(Glu56Asp)
-?/. - c.202-7T>A r.(=) p.(=)
-?/. - c.382G>T r.(?) p.(Ala128Ser)
-?/. - c.382G>T r.(?) p.(Ala128Ser)
?/. - c.481G>C r.(?) p.(Asp161His)
+/. - c.586C>T r.(?) p.(Gln196*)
+/. - c.586C>T r.(?) p.(Gln196*)
?/. - c.589-875A>G r.spl? p.(=)
-?/. - c.657+9A>C r.(=) p.(=)
+/. - c.763C>T r.(?) p.(Arg255*)
?/. - c.769_771del r.(?) p.(Glu257del)
?/. - c.950A>T r.(?) p.(Asp317Val)
+/. - c.1031_1034del r.(?) p.(Arg344LysfsTer2)
+/. 7 c.1116del r.1116del p.(Glu373Lysfs*29)
?/. - c.1280T>C r.(?) p.(Leu427Ser)
?/. - c.1280T>C r.(?) p.(Leu427Ser)
?/. - c.1301T>C r.(?) p.(Leu434Pro)
-/. - c.1517A>C r.(?) p.(Glu506Ala)
-/. - c.1517A>C r.(?) p.(Glu506Ala)
-/. - c.1517A>C r.(?) p.(Glu506Ala)
-/. - c.1527+6A>G r.(=) p.(=)
-?/. - c.1528-4dup r.spl? p.?
-?/. - c.1904C>G r.(?) p.(Ser635Cys)
+?/. 11 c.1938_1941del r.(?) p.(Arg647Lysfs*7)
-?/. - c.2029A>G r.(?) p.(Met677Val)
-?/. - c.2044T>C r.(?) p.(Leu682=)
?/. - c.2075A>G r.(?) p.(Gln692Arg)
-?/. - c.2102A>G r.(?) p.(Asn701Ser)
-?/. - c.2134G>A r.(?) p.(Glu712Lys)
-?/. - c.2134G>A r.(?) p.(Glu712Lys)
-?/. - c.2134G>A r.(?) p.(Glu712Lys)
-?/. - c.2494G>A r.(?) p.(Asp832Asn)
-?/. - c.2542A>G r.(?) p.(Ile848Val)
-?/. - c.2651A>G r.(?) p.(Asp884Gly)
?/. - c.2756T>C r.(?) p.(Ile919Thr)
?/. - c.2978T>C r.(?) p.(Ile993Thr)
+?/. 11 c.2993_2994del r.2993_2994del p.Lys998Serfs*5
+/. - c.2993_2994del r.(?) p.(Lys998Serfs*5)
?/. - c.3091G>A r.(?) p.(Glu1031Lys)
-?/. - c.3100C>T r.(?) p.(Leu1034Phe)
-?/. - c.3120A>G r.(?) p.(Ile1040Met)
?/. - c.3161T>G r.(?) p.(Val1054Gly)
?/. - c.3380C>T r.(?) p.(Ala1127Val)
+/. 11 c.3426dup r.3426dup p.Leu1143Ilefs*4
?/. - c.3704T>C r.(?) p.(Met1235Thr)
?/. - c.3823G>A r.(?) p.(Glu1275Lys)
?/. - c.4062A>C r.(?) p.(Lys1354Asn)
?/. - c.4139C>T r.(?) p.(Thr1380Ile)
-?/. - c.4159G>A r.(?) p.(Glu1387Lys)
+/. - c.4205_4206del r.(?) p.(Gln1402Argfs*8)
?/. - c.4297A>G r.(?) p.(Lys1433Glu)
+/. - c.4402dup r.(?) p.(Ile1468AsnfsTer19)
+?/. 11 c.4508_4511del r.(?) p.(Met1503Argfs*11)
?/. - c.4727G>A r.(?) p.(Arg1576His)
?/. - c.4727G>A r.(?) p.(Arg1576His)
-?/. - c.4727G>A r.(?) p.(Arg1576His)
?/. - c.4779T>G r.(?) p.(Asp1593Glu)
-?/. - c.4998A>G r.(?) p.(Val1666=)
-?/. - c.5086G>A r.(?) p.(Glu1696Lys)
-?/. - c.5137G>C r.(?) p.(Glu1713Gln)
-/. - c.5255G>A r.(?) p.(Arg1752Lys)
?/. - c.5260+5034A>T r.spl? p.(=)
-?/. - c.5298G>T r.(?) p.(Lys1766Asn)
?/. - c.5343-314T>C r.spl? p.(=)
-?/. - c.5372A>G r.(?) p.(His1791Arg)
?/. - c.5396G>C r.(?) p.(Arg1799Pro)
-?/. - c.5411G>A r.(?) p.(Arg1804Gln)
+/. - c.5420G>T r.(?) p.(Gly1807Val)
-/. - c.5479G>A r.(?) p.(Gly1827Ser)
?/. - c.5537C>T r.(?) p.(Thr1846Ile)
?/. - c.5537C>T r.(?) p.(Thr1846Ile)
-?/. - c.5544G>C r.(?) p.(Leu1848Phe)
-?/. - c.5629C>A r.(?) p.(Pro1877Thr)
-?/. - c.5651A>G r.(?) p.(His1884Arg)
-?/. - c.5657T>C r.(?) p.(Met1886Thr)
-?/. - c.5738C>G r.(?) p.(Ser1913Cys)
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