Transcript #00025357 (NM_003075.3, SMARCC2 gene)

Transcript name transcript variant 1
Gene name SMARCC2 (SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2)
Chromosome 12
Transcript - NCBI ID NM_003075.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_003066.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2018-12-28 13:49:15 +01:00 (CET)
Date last edited N/A


Variants

110 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-102_-81del r.(?) p.(=)
+?/. _1_28_ c.-106_*1837{0} r.0 p.0
-?/. - c.53C>G r.(?) p.(Ala18Gly)
+?/. - c.172C>T r.(?) p.(Gln58Ter)
+?/. - c.230C>T r.(?) p.(Pro77Leu)
+?/. - c.230C>T r.(?) p.(Pro77Leu)
+?/. - c.230C>T r.(?) p.(Pro77Leu)
+?/. - c.230C>T r.(?) p.(Pro77Leu)
-?/. - c.231+280G>A r.(=) p.(=)
+?/. - c.317+2T>A r.spl p.?
?/. - c.317+2T>A r.spl? p.?
+?/. - c.326dup r.(?) p.(Tyr109Ter)
+?/. - c.326dup r.(?) p.(Tyr109Ter)
+?/. - c.327C>G r.(?) p.(Tyr109Ter)
+?/. - c.327C>G r.(?) p.(Tyr109Ter)
?/. - c.327C>G r.(?) p.(Tyr109Ter)
?/. - c.327C>G r.(?) p.(Tyr109Ter)
?/. - c.359A>G r.(?) p.(Asn120Ser)
?/. - c.368T>C r.(?) p.(Met123Thr)
./. - c.400A>G r.(?) p.(Asn134Asp)
-?/. - c.492+5A>G r.spl? p.?
-?/. - c.492+5A>G r.spl? p.?
?/. - c.529G>A r.(?) p.(Val177Ile)
+?/. - c.574C>T r.(?) p.(Arg192Ter)
+?/. - c.574C>T r.(?) p.(Arg192Ter)
?/. - c.574C>T r.(?) p.(Arg192Ter)
+?/. - c.640A>G r.(?) p.(Thr214Ala)
+?/. - c.723G>A r.(?) p.(Trp241Ter)
+/. - c.723G>A r.(?) p.(Trp241*)
+?/. - c.743T>C r.(?) p.(Phe248Ser)
?/. - c.793C>T r.(?) p.(Pro265Ser)
+?/. - c.805C>T r.(?) p.(Arg269Ter)
+?/. - c.805C>T r.(?) p.(Arg269Ter)
+?/. 10 c.880_881del r.(?) p.(Gly294LysfsTer3)
+?/. 10 c.888_889del r.(?) p.(Tyr296Ter)
?/. - c.956+3G>A r.spl? p.?
+/. - c.999dup r.(?) p.(Glu334Argfs*49)
-?/. - c.1008A>G r.(?) p.(Gln336=)
-?/. - c.1052A>G r.(?) p.(Asn351Ser)
+?/. - c.1094_1097del r.(?) p.(Lys365Thrfs*12)
-?/. - c.1127C>T r.(?) p.(Thr376Ile)
-?/. - c.1141+10G>C r.(=) p.(=)
?/. - c.1141+10_1141+11insTC r.(=) p.(=)
?/. - c.1173G>A r.(?) p.(=)
-?/. - c.1311-3C>G r.spl p.?
+?/. - c.1311-1G>A r.spl p.?
+?/. - c.1327C>T r.(?) p.(Arg443Trp)
?/. - c.1327C>T r.(?) p.(Arg443Trp)
?/. - c.1355G>A r.(?) p.(Gly452Asp)
+?/. - c.1397G>C r.(?) p.(Arg466Pro)
-?/. - c.1493T>C r.(?) p.(Met498Thr)
+/. 16i c.1496+1G>T r.[1496_1497ins[T;1496+2_1496+126],1383_1496del] p.[Met498_Arg499insSWVLWLRGRGYMRMPAYGCVLATVEMPARNTEEQTEKSTSRE,Ile461_Arg499delinsMet]
?/. - c.1497-3C>G r.spl? p.?
+/. 17 c.1555C>T r.(?) p.(Arg519*)
?/. - c.1650+2T>C r.spl? p.?
+/. - c.1651-2A>G r.spl p.?
-?/. - c.1683T>C r.(?) p.(Phe561=)
+/. - c.1770+1G>T r.spl p.?
-?/. - c.1781C>T r.(?) p.(Ala594Val)
+?/. - c.1796G>A r.(?) p.(Arg599His)
?/. - c.1801T>C r.(?) p.(Trp601Arg)
+?/. - c.1824_1826del r.(?) p.(Leu610del)
+/. 19 c.1826T>C r.(?) p.(Leu609Pro)
+/. - c.1826T>C r.(?) p.(Leu609Pro)
+/. - c.1829T>C r.(?) p.(Leu610Pro)
+/. - c.1829T>C r.(?) p.(Leu610Pro)
+/. - c.1833+1G>T r.(1771_1833del) p.?
+/. - c.1833+2T>C r.spl p.?
+/. - c.1833+2T>C r.spl p.?
+?/. - c.1833+2T>C r.spl? p.?
-?/. - c.1833+5T>C r.spl? p.?
+?/. - c.1834-7C>G r.(?) p.Glu611_Ala612insHisGln
+/. - c.1838T>C r.(?) p.(Leu613Pro)
+?/. - c.1849_1854del r.(?) p.(Lys617_Asp618del)
+?/. - c.1877_1878insAAGTG r.(?) p.(His626Glnfs*33)
+/. - c.1903T>C r.(?) p.(Cys635Arg)
+?/. - c.1919T>C r.(?) p.(Leu640Pro)
+?/. - c.2059C>T r.(?) p.(Arg687Ter)
+?/. - c.2059C>T r.(?) p.(Arg687Ter)
+/. - c.2074G>C r.(?) p.(Ala692Pro)
?/. - c.2234C>T r.(?) p.(Ser745Phe)
+/. - c.2320-2A>G r.spl? p.?
-?/. - c.2413G>A r.(?) p.(Asp805Asn)
-?/. - c.2452A>G r.(?) p.(Ile818Val)
+?/. - c.2464G>T r.(?) p.(Glu822*)
+?/. - c.2602G>C r.(?) p.(Ala868Pro)
+?/. - c.2639A>G r.(?) p.(Glu880Gly)
+?/. - c.2678A>G r.(?) p.(Glu893Gly)
+/. - c.2686A>G r.(?) p.(Met896Val)
+?/. - c.2697G>T r.(?) p.(Leu899Phe)
+/. - c.2699A>G r.(?) p.(Glu900Gly)
-?/. - c.2954G>C r.(?) p.(Gly985Ala)
?/. - c.3067C>A r.(?) p.(Gln1023Lys)
-?/. - c.3089C>T r.(?) p.(Ala1030Val)
+?/. - c.3094dup r.(?) p.(Gln1032ProfsTer45)
-?/. - c.3127C>G r.(?) p.(Pro1043Ala)
+/. - c.3129del r.(?) p.(Gly1044Aspfs*17)
+?/. - c.3129del r.(?) p.(Gly1044AspfsTer17)
+?/. - c.3129del r.(?) p.(Gly1044AspfsTer17)
+?/. - c.3135_3139dup r.(?) p.](Gly1047AlafsTer16),?]
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