Transcript #00008204 (NM_004960.3, FUS gene)

Transcript name transcript variant 1
Gene name FUS (fused in sarcoma)
Chromosome 16
Transcript - NCBI ID NM_004960.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_004951.1
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

342 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-4008385_*685925dup - -
+?/. - c.-3091535_*3397241del r.0? p.0?
-/. - c.-54A>G r.(=) p.(=)
-?/. - c.6C>T r.(?) p.(Ala2=)
-?/. - c.52C>A r.(?) p.(Pro18Thr)
?/. - c.52C>T r.(?) p.(Pro18Ser)
?/. 3 c.52C>T r.(?) p.(Pro18Ser)
+/? 3 c.52C>T r.(?) p.(Pro18Ser)
+/? 4 c.52C>T r.(?) p.(Pro18Ser)
-/? 3 c.(62C>A) r.(?) p.(Pro21His)
-?/. - c.132C>T r.(?) p.(Ser44=)
-/? 3 c.(147C>A) r.(?) p.(=)
-/. - c.147C>A r.(?) p.(Gly49=)
-/. - c.147C>A r.(=) p.(=)
-/. - c.147C>A r.(?) p.(Gly49=)
-/. - c.147C>A r.(?) p.(Gly49=)
-/. - c.147C>A r.(?) p.(Gly49=)
-/. - c.147C>A r.(?) p.(Gly49=)
-/? 3 c.(153C>T) r.(?) p.(=)
-/. - c.153C>T r.(?) p.(Gly51=)
-/. - c.153C>T r.(?) p.(Gly51=)
+/+ 3 c.(170_172del) r.(?) p.(Ser57del)
+/? 3 c.170_172del r.(?) p.(Ser57del)
-/? 3 c.(188A>G) r.(?) p.(Asn63Ser)
-?/. - c.188A>G r.(?) p.(Asn63Ser)
-/. - c.190+9T>C r.(=) p.(=)
-/. - c.190+9T>C r.(=) p.(=)
-?/. - c.191-32C>G r.(=) p.(=)
-?/. - c.198T>C r.(?) p.(Tyr66=)
-?/. - c.198T>C r.(?) p.(Tyr66=)
-?/. - c.236G>A r.(?) p.(Gly79Asp)
?/. - c.265T>A r.(?) p.(Ser89Thr)
?/. - c.265T>A r.(?) p.(Ser89Thr)
+/? 4 c.287_291delinsAT r.(?) p.(Ser96del)
-/. - c.291C>T r.(?) p.(Tyr97=)
-/. - c.291C>T r.(=) p.(=)
-/. - c.291C>T r.(?) p.(Tyr97=)
-/. - c.291C>T r.(?) p.(Tyr97=)
-/. - c.291C>T r.(?) p.(Tyr97=)
-/. - c.291C>T r.(?) p.(Tyr97=)
?/. - c.292C>A r.(?) p.(Pro98Thr)
-?/. - c.336-19_336-18insG r.(=) p.(=)
+/? 4 c.344G>A r.(?) p.(Ser115Asn)
?/. - c.350C>T r.(?) p.(Ser117Phe)
?/. - c.365A>G r.(?) p.(Tyr122Cys)
-?/. - c.375C>G r.(?) p.(Pro125=)
-?/. - c.404G>A r.(?) p.(Ser135Asn)
+/. - c.430_447del r.(?) p.(Gly144_Tyr149del)
?/. - c.430_447del r.(?) p.(Gly144_Tyr149del)
+/? 5 c.430_447del r.(?) p.(Gly144_Tyr149del)
+/? 6 c.430_447del r.(?) p.(Gly144_Tyr149del)
?/. - c.434A>G r.(?) p.(Gln145Arg)
+/+ 5 c.(467G>A) r.(?) p.(Gly156Glu)
+/? 5 c.467G>A r.(?) p.(Gly156Glu)
?/. - c.491G>C r.(?) p.(Ser164Thr)
-?/. - c.498T>A r.(?) p.(Gly166=)
-/? 5_5i c.515_523+3del r.(?) p.?
?/. - c.515_523+3del r.spl? p.?
?/. - c.521G>A r.(?) p.(Gly174Glu)
-/. - c.521_523+3del r.spl? p.?
-/. - c.521_523+3del r.spl? p.?
-?/. - c.521_523+3del r.spl? p.?
-/- 5_5i c.521_523+3del r.(?) p.?
+/? 5 c.521_523+3del r.(?) p.(Gly174_Gly175del)
+/? 6 c.521_523+3del r.(?) p.(Gly174_Gly175del)
-?/. - c.521_523+3del r.spl? p.?
-?/. - c.521_523+3dup r.spl? p.?
+/+ 5 c.523+3_523+4insGGAGGT r.(?) p.(=)
-/. - c.523+22C>T r.(=) p.(=)
-/. - c.523+59del r.(=) p.(=)
-?/. - c.524-24del r.(=) p.(=)
-?/. - c.524-13dup r.(=) p.(=)
-?/. - c.524-5C>T r.spl? p.?
?/. - c.537A>C r.(?) p.(Gln179His)
+/? 6 c.559G>A r.(?) p.(Gly187Ser)
?/? 6 c.(571G>A) r.(?) p.(Gly191Ser)
+/? 6 c.571G>A r.(?) p.(Gly191Ser)
-?/. - c.576C>T r.(?) p.(Gly192=)
+/? 6 c.616G>A r.(?) p.(Gly206Ser)
-/? 6 c.(630G>C) r.(?) p.(Gln210His)
?/. - c.630G>C r.(?) p.(Gln210His)
-/. - c.630G>C r.(?) p.(Gln210His)
-?/. - c.633G>C r.(?) p.(Gln211His)
?/? 6 c.(646C>T) r.(?) p.(Arg216Cys)
?/. - c.646C>T r.(?) p.(Arg216Cys)
?/. - c.646C>T r.(?) p.(Arg216Cys)
+/? 6 c.646C>T r.(?) p.(Arg216Cys)
-?/. - c.654_662del r.(?) p.(Arg218_Gly220del)
-?/. - c.660C>G r.(?) p.(Gly220=)
?/. - c.661_663del r.(?) p.(Ser221del)
?/. - c.671_672insTGG r.(?) p.(Gly231dup)
+/+ 6 c.(674G>T) r.(?) p.(Gly225Val)
+/? 6 c.674G>T r.(?) p.(Gly225Val)
-?/. - c.675C>T r.(?) p.(Gly225=)
-?/. - c.675C>T r.(?) p.(Gly225=)
-/? 6 c.(676G>A) r.(?) p.(Gly226Ser)
-/? 6 c.(678_686del) r.(?) p.(Gly229_Gly231del)
?/. - c.679G>A r.(?) p.(Gly227Ser)
-/? 6 c.(681_686del) r.(?) p.(Gly230_Gly231del)
-/? 6 c.(681_686dup) r.(?) p.(Gly230_Gly231dup)
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