Transcript #00025666 (NM_001127208.2, TET2 gene)

Transcript name transcript variant 1
Gene name TET2 (tet methylcytosine dioxygenase 2)
Chromosome 4
Transcript - NCBI ID NM_001127208.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001120680.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2021-12-17 14:22:16 +01:00 (CET)
Date last edited N/A


Variants

56 entries on 1 page. Showing entries 1 - 56.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-193+19T>C r.(=) p.(=)
?/. - c.100C>T r.(?) p.(Leu34Phe)
?/. - c.100C>T r.(?) p.(Leu34Phe)
-?/. - c.100C>T r.(?) p.(Leu34Phe)
-?/. - c.192C>T r.(?) p.(Pro64=)
?/. - c.652G>A r.(?) p.(Val218Met)
?/. - c.652G>A r.(?) p.(Val218Met)
+/. - c.685dup r.(?) p.(Thr229Asnfs*25)
-?/. - c.837C>T r.(?) p.(Thr279=)
-?/. - c.972A>G r.(?) p.(Gln324=)
?/. - c.1064G>A r.(?) p.(Gly355Asp)
-?/. - c.1064G>A r.(?) p.(Gly355Asp)
-?/. - c.1794T>A r.(?) p.(Asn598Lys)
+?/. 3 c.2218C>T r.(?) p.(Gln740Ter)
-?/. - c.2440C>T r.(?) p.(Arg814Cys)
-?/. - c.2440C>T r.(?) p.(Arg814Cys)
?/. - c.2441G>A r.(?) p.(Arg814His)
+/. - c.2461C>T r.(?) p.(Gln821*)
+?/. - c.2474C>G r.(?) p.(Ser825*)
?/. - c.2599T>C r.(?) p.(Tyr867His)
-?/. - c.2599T>C r.(?) p.(Tyr867His)
-?/. - c.2604T>G r.(?) p.(Phe868Leu)
-?/. - c.2868C>G r.(?) p.(Leu956=)
-?/. - c.2941A>G r.(?) p.(Ile981Val)
+?/. - c.2974del r.(?) p.(Cys992Valfs*15)
-?/. - c.3116C>T r.(?) p.(Ser1039Leu)
-?/. - c.3117G>A r.(?) p.(Ser1039=)
+/. - c.3217del r.(?) p.(Glu1073Asnfs*9)
-?/. - c.3251A>C r.(?) p.(Gln1084Pro)
-?/. - c.3251A>C r.(?) p.(Gln1084Pro)
-?/. - c.3409+15T>A r.(=) p.(=)
-?/. - c.3409+52A>G r.(=) p.(=)
-?/. - c.3500+336A>G r.(=) p.(=)
?/. - c.3578G>T r.(?) p.(Cys1193Phe)
?/. - c.3583A>G r.(?) p.(Ile1195Val)
-?/. - c.3595-4G>A r.spl? p.?
+/. - c.3767_3771dup r.(?) p.(Leu1258Alafs*10)
?/. - c.3790G>A r.(?) p.(Ala1264Thr)
-?/. - c.3954+3T>G r.spl? p.?
-?/. - c.4140T>C r.(?) p.(His1380=)
?/. 9 c.4161C>T r.(?) p.(Asn1387=)
+/. - c.4183-1G>A r.spl? p.?
?/. - c.4249G>A r.(?) p.(Val1417Ile)
-?/. - c.4354C>A r.(?) p.(Arg1452=)
-?/. - c.4776C>T r.(?) p.(Thr1592=)
-?/. - c.4926C>T r.(?) p.(Cys1642=)
-?/. - c.5035T>C r.(?) p.(Tyr1679His)
-?/. - c.5103G>A r.(?) p.(Met1701Ile)
-?/. - c.5152G>T r.(?) p.(Val1718Leu)
-?/. - c.5167C>T r.(?) p.(Pro1723Ser)
-/. - c.5284A>G r.(?) p.(Ile1762Val)
?/. - c.5333A>G r.(?) p.(His1778Arg)
?/. - c.5333A>G r.(?) p.(His1778Arg)
-?/. - c.5333A>G r.(?) p.(His1778Arg)
?/. - c.5576T>C r.(?) p.(Ile1859Thr)
?/. - c.5890T>C r.(?) p.(Tyr1964His)
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