Transcript #00000271 (NM_015294.3, TRIM37 gene)

Transcript name transcript variant 1
Gene name TRIM37 (tripartite motif containing 37)
Chromosome 17
Transcript - NCBI ID NM_015294.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_056109.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-08-28 13:02:13 +02:00 (CEST)
Date last edited N/A


Variants

79 entries on 1 page. Showing entries 1 - 79.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.(?_-45419)_(2695+3579_2696-1)del r.0? p.0?
+/+ 2 c.81del r.(?) p.(Cys28Valfs*17)
?/. - c.92G>A r.(?) p.(Cys31Tyr)
-?/. - c.124-9C>A r.(=) p.(=)
+?/. - c.164+3_164+6del r.(?) p.(?)
+?/. - c.164+3_164+6del r.(?) p.(?)
+?/+? 4 c.181C>T r.(?) p.(Arg61*)
+?/+? 4 c.181C>T r.(?) p.(Arg61*)
+?/+? 4 c.181C>T r.(?) p.(Arg61*)
-?/. - c.219A>G r.(?) p.(Thr73=)
+/+ 4 c.227T>C r.(227u>c) p.(Leu76Pro)
+/+ 5 c.326G>C r.(326g>c) p.(Cys109Ser)
-?/. - c.398C>T r.(?) p.(Ala133Val)
-?/. - c.398C>T r.(?) p.(Ala133Val)
+/+ 6i c.493-2A>G r.493_497delgaaag p.Arg166Cysfs*10
?/. - c.572C>G r.(?) p.(Ala191Gly)
+?/+? 8i_9i c.685-233_810-2895del r.? p.(Leu229*)
+?/+? 8i_9i c.685-233_810-2895del r.? p.(Leu229*)
+/+ 9 c.685-?_809+?del r.(685_809del) p.(Leu229*)
-?/. - c.737T>C r.(?) p.(Met246Thr)
+/+ 9 c.745C>T r.(745c>u) p.(Gln249*)
-?/. - c.810-3del r.spl? p.?
-/. - c.810-3del r.spl? p.?
+/+ 9i c.810-1G>A r.810_817delugaauuag p.Glu271Alafs*64
?/. - c.821C>G r.(?) p.(Pro274Arg)
?/. - c.821C>G r.(?) p.(Pro274Arg)
+/+ 10 c.838_842del r.838_842delacuuu p.Thr280Cysfs*56
+/+ 10 c.860G>A r.810_860del p.Glu271_Ser287del
-?/. - c.861-6C>T r.(=) p.(=)
-?/. - c.861C>G r.(?) p.(Ser287Arg)
+/+ 12 c.965G>T r.965g>u p.Gly322Val
+/+ 13 c.1037_1040dup r.(1037_1040dupagau) p.(Met347Ilefs*8)
+?/. 13 c.1153_1154insGACTTACTCGC r.(?) p.(Ala385GlyfsTer10)
+?/+? 13 c.1166A>G r.(1166a>g) p.(Tyr389Cys)
+/+ 14 c.1233del r.(?) p.(Lys411Asnfs*23)
+/+ 14i_16i c.1314+507_1668-207del r.(1315_1667del) p.(Arg439Valfs*5)
+?/+? 14i_16i c.1314+782_1668-221del r.? p.(Arg439Valfs*5)
?/. - c.1337G>A r.(?) p.(Arg446Gln)
+/+ 15 c.1346dup r.1346dupa p.Ser450Valfs*9
-?/. - c.1357T>A r.(?) p.(Leu453Met)
-?/. - c.1386C>A r.(?) p.(Pro462=)
+/+ 15 c.1411C>T r.(1411c>u) p.(Arg471*)
-?/. - c.1412G>A r.(?) p.(Arg471Gln)
?/. - c.1447G>A r.(?) p.(Glu483Lys)
?/. - c.1532A>T r.(?) p.(His511Leu)
?/. - c.1533C>G r.(?) p.(His511Gln)
?/. - c.1536_1537insAT r.(?) p.(Leu513IlefsTer17)
?/. - c.1538_1540del r.(?) p.(Leu513_Ser514delinsPro)
-?/. - c.1570T>G r.(?) p.(Tyr524Asp)
?/. - c.1630A>G r.(?) p.(Ser544Gly)
?/. - c.1717G>A r.(?) p.(Glu573Lys)
-?/. - c.1748C>A r.(?) p.(Pro583His)
-?/. - c.1754-3C>T r.spl? p.?
?/. - c.1754-3C>T r.spl? p.?
+/+ 18 c.1894_1895del r.(?) p.(Glu632Lysfs*25)
+/+ 18 c.1910_1911dup r.(?) p.(Gln638Tyrfs*36)
?/. - c.1919G>A r.(?) p.(Arg640His)
?/. - c.1919G>A r.(?) p.(Arg640His)
+?/+? 18i c.1949-12A>G r.1948_1949ins1949-11_1949-1 p.Ala650Valfs*27
+/+ 19 c.1999C>T r.(1999c>u) p.(Arg667*)
-?/. - c.2047G>A r.(?) p.(Ala683Thr)
+/+ 19 c.2056C>T r.(2056c>u) p.(Arg686*)
+/+ 19 c.2125del r.(?) p.(Met709Cysfs*60)
+/+ 19 c.2212del r.2212delg p.Glu738Asnfs*31
-?/. - c.2240A>G r.(?) p.(Asn747Ser)
-?/. - c.2240A>G r.(?) p.(Asn747Ser)
-?/. - c.2283C>G r.(?) p.(Pro761=)
-?/. - c.2387-7T>C r.(=) p.(=)
-?/. - c.2430C>T r.(?) p.(=)
+?/+? 21 c.2437_2438insAT r.(?) p.(Leu813Tyrfs*2)
+/+ 21 c.2438_2439insAT r.(2438_2439insau) p.(Ile814*)
-?/. - c.2454C>T r.(?) p.(Ile818=)
-?/. - c.2512G>A r.(?) p.(Val838Ile)
-?/. - c.2512G>C r.(?) p.(Val838Leu)
?/. - c.2707G>A r.(?) p.(Asp903Asn)
?/. - c.2746G>A r.(?) p.(Glu916Lys)
-?/. - c.2813-10T>G r.(=) p.(=)
-?/. - c.*18561G>A r.(=) p.(=)
-?/. - c.*18696A>G r.(=) p.(=)
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