Transcript #00021818 (NM_012210.3, TRIM32 gene)

Transcript name transcript variant 1
Gene name TRIM32 (tripartite motif containing 32)
Chromosome 9
Transcript - NCBI ID NM_012210.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_036342.2
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

226 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-261524T>C r.(?) p.(=)
-?/. - c.-35752C>T r.(?) p.(=)
-?/. - c.-712T>C r.(?) p.(=)
+/. _1_2_ c.(?_-161)_(*1596_?)del r.0 p.0
-/. - c.-133G>C r.(?) p.(=)
-?/. - c.-81-291A>G r.(=) p.(=)
+/. _1_2_ c.(?-161)_(*1596_?)del r.0 p.0
+/. - c.(?_-82+3795)_*1596{0} r.? p.0?
?/. - c.1A>G r.(?) p.(Met1?)
-?/. - c.6T>G r.(?) p.(=)
-?/. - c.6T>V r.(?) p.(Ala2=)
?/. 2 c.24C>A r.(?) p.(His8Gln)
?/. - c.59G>T r.(?) p.(Cys20Phe)
?/. 2 c.90G>A r.(?) p.(=)
?/. 2 c.90G>A r.(?) p.(=)
?/. 2 c.98G>A r.(?) p.(Arg33His)
?/. 2 c.127A>G r.(?) p.(Ile43Val)
-/. - c.201T>C r.(?) p.(Ile67=)
-?/. - c.276C>T r.(?) p.(Ser92=)
?/. - c.276C>T r.(?) p.(Ser92=)
?/. - c.276C>T r.(?) p.(Ser92=)
-?/. - c.279G>A r.(?) p.(Glu93=)
?/. 2 c.292C>A r.(?) p.(Leu98Ile)
?/. - c.314G>T r.(?) p.(Arg105Leu)
?/. - c.317G>A r.(?) p.(Arg106His)
-?/. - c.330A>G r.(?) p.(Gln110=)
-?/. - c.338G>A r.(?) p.(Arg113Gln)
?/. 2 c.339G>C r.(?) p.(=)
?/. 2 c.370C>T r.(?) p.(Arg124Trp)
?/. - c.382C>T r.(?) p.(His128Tyr)
+/. 2 c.388C>T r.(?) p.(Pro130Ser)
+/. 2 c.388C>T r.(?) p.(Pro130Ser)
+/. 2 c.388C>T r.(?) p.(Pro130Ser)
-?/. - c.404C>T r.(?) p.(Thr135Ile)
?/. - c.404C>T r.(?) p.(Thr135Ile)
?/. 2 c.413T>G r.(?) p.(Val138Gly)
?/. 2 c.430G>A r.(?) p.(Glu144Lys)
+/. - c.459_462dup r.(?) p.(Arg155Asnfs*29)
?/. 2 c.464G>A r.(?) p.(Arg155His)
+?/. - c.467T>C r.(?) p.(Leu156Pro)
?/. - c.467T>C r.(?) p.(Leu156Pro)
?/. - c.467T>C r.(?) p.Leu156Pro
-/. - c.479T>C r.(?) p.(Met160Thr)
?/. - c.479_480insA r.(?) p.(Met160IlefsTer23)
?/. 2 c.480G>A r.(?) p.(Met160Ile)
?/. 2 c.480G>A r.(?) p.(Met160Ile)
?/. 2 c.480G>A r.(?) p.(Met160Ile)
?/. 2 c.480G>A r.(?) p.(Met160Ile)
?/. 2 c.480G>A r.(?) p.(Met160Ile)
?/. - c.488T>C r.(?) p.(Leu163Pro)
+?/. - c.488T>C r.(?) p.(Leu163Pro)
+?/. - c.488T>C r.(?) p.(Leu163Pro)
?/. - c.496C>T r.(?) p.(Arg166Trp)
?/. 2 c.496C>T r.(?) p.(Arg166Trp)
?/. 2 c.497G>A r.(?) p.(Arg166Gln)
?/. - c.497G>A r.(?) p.(Arg166Gln)
?/. - c.497G>A r.(?) p.(Arg166Gln)
?/. - c.497G>A r.(?) p.(Arg166Gln)
-?/. - c.501G>A r.(?) p.(Lys167=)
-?/. - c.501G>A r.(?) p.(Lys167=)
+/. 2 c.509T>A r.(?) p.(Leu170*)
?/. - c.521C>T r.(?) p.(Ser174Phe)
?/. 2 c.521C>T r.(?) p.(Ser174Phe)
?/. - c.521C>T r.(?) p.(Ser174Phe)
?/. - c.521C>T r.(?) p.(Ser174Phe)
?/. - c.521C>T r.(?) p.(Ser174Phe)
-?/. - c.521C>T r.(?) p.(Ser174Phe)
?/. 2 c.524A>G r.(?) p.(Lys175Arg)
+/. - c.542_543insAAAGGTA r.(?) p.(Tyr181*)
?/. 2 c.558G>C r.(?) p.(Gln186His)
?/. 2 c.558G>C r.(?) p.(Gln186His)
?/. - c.558G>C r.(?) p.(Gln186His)
?/. - c.558G>C r.(?) p.(Gln186His)
-?/. - c.558G>C r.(?) p.(Gln186His)
?/. 2 c.558G>C r.(?) p.(Gln186His)
?/. 2 c.558G>C r.(?) p.(Gln186His)
?/. 2 c.558G>C r.(?) p.(Gln186His)
?/. 2 c.558G>C r.(?) p.(Gln186His)
?/. 2 c.558G>C r.(?) p.(Gln186His)
?/. 2 c.558G>C r.(?) p.(Gln186His)
?/. - c.558G>C r.(?) p.(Gln186His)
?/. - c.558G>C r.(?) p.(Gln186His)
?/. - c.558G>C r.(?) p.(Gln186His)
?/. - c.558G>C r.(?) p.(Gln186His)
?/. - c.558G>C r.(?) p.(Gln186His)
?/. - c.558G>C r.(?) p.(Gln186His)
+/. - c.574dup r.(?) p.(Glu192Glyfs*7)
+/. - c.574dup r.(?) p.(Glu192Glyfs*7)
?/. - c.607C>T r.(?) p.(Arg203Trp)
-/. 5i c.627+18T>G r.(?) p.(=)
?/. 2 c.650A>G r.(?) p.(Asn217Ser)
-/. 6 c.651T>C r.(?) p.(=)
?/. - c.688A>G r.(?) p.(Ile230Val)
+/. 2 c.691del r.(?) p.(Ala231Glnfs*21)
+/. - c.691del r.(?) p.(Ala231Glnfs*21)
?/. 2 c.700C>A r.(?) p.(Gln234Lys)
+?/. - c.712C>T r.(?) p.(Arg238Cys)
?/. - c.712C>T r.(?) p.(Arg238Cys)
+?/. - c.722A>G r.(?) p.(Tyr241Cys)
?/. - c.743A>C r.(?) p.(Gln248Pro)
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