Transcript #00024173 (NM_138927.2, SON gene)

Transcript name transcript variant f
Gene name SON (SON DNA binding protein)
Chromosome 21
Transcript - NCBI ID NM_138927.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_620305.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-10-06 22:31:40 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_12_ c.-55_*1090[0] r.0 p.0
+/. _1_12_ c.-55_*1090[0] r.0 p.0
+/. _1_12_ c.-55_*1090[0] r.0 p.0
+/. - c.-55_*1090[0] r.0 p.0
+/. _1_12_ c.-55_*1090{0} r.0? p.0?
-?/. - c.137C>T r.(?) p.(Ala46Val)
-?/. - c.138G>A r.(?) p.(Ala46=)
+/. 3 c.268del r.(?) p.(Ser90Valfs*59)
+/. - c.268del r.(?) p.(Ser90Valfs*59)
+/. - c.286C>T r.(?) p.(Gln96*)
-?/. - c.335A>G r.(?) p.(Lys112Arg)
+/. - c.348_351del r.(?) p.(Asn116Lysfs*32)
-?/. - c.359A>G r.(?) p.(Lys120Arg)
+/. - c.384del r.(?) p.(Lys128Asnfs*21)
+/. - c.394C>T r.(?) p.(Gln132*)
+/. - c.457del r.(?) p.(Asp153Ilefs*4)
-?/. - c.497C>T r.(?) p.(Ala166Val)
-?/. - c.607G>C r.(?) p.(Glu203Gln)
-?/. - c.657A>G r.(?) p.(Thr219=)
+/. - c.668C>T r.(?) p.(Ser223Leu)
?/. - c.668C>T r.(?) p.(Ser223Leu)
-?/. - c.737C>T r.(?) p.(Ala246Val)
-?/. - c.763C>G r.(?) p.(Leu255Val)
?/. - c.850_861del r.(?) p.(Pro284_Ser287del)
-?/. - c.978G>A r.(?) p.(Met326Ile)
-?/. - c.1000A>G r.(?) p.(Ile334Val)
-?/. - c.1007C>T r.(?) p.(Ala336Val)
-?/. - c.1035C>T r.(?) p.(Asp345=)
?/. - c.1052C>G r.(?) p.(Ala351Gly)
?/. - c.1199C>T r.(?) p.(Thr400Ile)
-?/. - c.1267C>T r.(?) p.(Pro423Ser)
?/. - c.1389_1409dup r.(?) p.(Gln467_Pro473dup)
-?/. - c.1390G>A r.(?) p.(Glu464Lys)
-?/. - c.1398A>T r.(?) p.(Pro466=)
-?/. - c.1412A>G r.(?) p.(Glu471Gly)
+/. - c.1444del r.(?) p.(Leu482Cysfs*4)
?/. - c.1650_1685del r.(?) p.(Val553_Pro564del)
-?/. - c.1664C>T r.(?) p.(Thr555Met)
-?/. - c.1664C>T r.(?) p.(Thr555Met)
-?/. - c.1670C>T r.(?) p.(Ala557Val)
+/. - c.1715T>A r.(?) p.(Leu572*)
+/. - c.1736C>G r.(?) p.(Thr579Ser)
-?/. - c.1792G>A r.(?) p.(Gly598Arg)
-?/. - c.1793G>A r.(?) p.(Gly598Glu)
+/. - c.1881_1882del r.(?) p.(Val629Alafs*56)
+/. 3 c.1881_1882del r.(?) p.(Val629Alafs*56)
+?/. - c.1979del r.(?) p.(Thr660Lysfs*8)
-?/. - c.2080A>G r.(?) p.(Thr694Ala)
?/. - c.2166_2168dup r.(?) p.(Thr723dup)
-?/. - c.2166_2168dup r.(?) p.(Thr723dup)
-?/. - c.2206C>G r.(?) p.(Leu736Val)
?/. - c.2236C>A r.(?) p.(Leu746Ile)
-?/. - c.2236C>A r.(?) p.(Leu746Ile)
?/. - c.2240C>T r.(?) p.(Ala747Val)
?/. - c.2305A>G r.(?) p.(Ser769Gly)
-?/. - c.2362A>G r.(?) p.(Thr788Ala)
-?/. - c.2364T>C r.(?) p.(Thr788=)
+/. 3 c.2365del r.(?) p.(Ser789Alafs*8)
?/. - c.2367C>A r.(?) p.(Ser789Arg)
?/. - c.2390C>G r.(?) p.(Ala797Gly)
?/. - c.2401A>G r.(?) p.(Met801Val)
-?/. - c.2422A>G r.(?) p.(Thr808Ala)
-?/. - c.2443A>C r.(?) p.(Met815Leu)
-?/. - c.2443A>C r.(?) p.(Met815Leu)
-?/. - c.2581A>G r.(?) p.(Met861Val)
?/. - c.2592G>C r.(?) p.(Gln864His)
-?/. - c.2611A>G r.(?) p.(Met871Val)
?/. - c.2655G>A r.(?) p.(Met885Ile)
+/. 3 c.2680C>T r.(?) p.(Gln894*)
?/. - c.2734G>C r.(?) p.(Asp912His)
+/. - c.2763C>A r.(?) p.(Tyr921Ter)
-?/. - c.2918C>T r.(?) p.(Ala973Val)
-?/. - c.2918C>T r.(?) p.(Ala973Val)
-?/. - c.3012T>C r.(?) p.(Ala1004=)
-?/. - c.3012T>C r.(?) p.(Ala1004=)
+/. - c.3038dup r.(?) p.(Tyr1013*)
-?/. - c.3039C>T r.(?) p.(Tyr1013=)
?/. - c.3070A>G r.(?) p.(Met1024Val)
+/. - c.3073dup r.(?) p.(Met1025Asnfs*6)
-?/. - c.3129_3152del r.(?) p.(Ala1044_Ser1051del)
+/. - c.3203C>G r.? p.(Ser1068*)
?/. - c.3204_3227del r.(?) p.(Ala1069_Ser1076del)
?/. - c.3235G>T r.(?) p.(Ala1079Ser)
+/. 3 c.3281dup r.(?) p.(Ser1095Valfs*6)
-?/. - c.3307A>G r.(?) p.(Met1103Val)
-?/. - c.3326C>T r.(?) p.(Ala1109Val)
-?/. - c.3326C>T r.(?) p.(Ala1109Val)
+/. - c.3334C>T r.(?) p.(Arg1112*)
+/. 3 c.3334C>T r.(?) p.(Arg1112*)
+/. - c.3449del r.(?) p.(Pro1150Leufs*18)
-?/. - c.3477G>A r.(?) p.(Pro1159=)
+/. 3 c.3597_3598dup r.(?) p.(Pro1200Argfs*17)
?/. - c.3650A>T r.(?) p.(Gln1217Leu)
-?/. - c.3688_3741dup r.(?) p.(Tyr1230_Thr1247dup)
-?/. - c.3688_3741dup r.(?) p.(Tyr1230_Thr1247dup)
+/. - c.3711del r.(?) p.(Ser1238Glnfs*3)
+/. - c.3711del r.(?) p.(Ser1238Glnfs*3)
+/. - c.3711del r.(?) p.(Ser1238GlnfsTer3)
-?/. - c.3726A>G r.(?) p.(Ser1242=)
?/. - c.3772T>G r.(?) p.(Ser1258Ala)
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