Transcript #00013143

Transcript name transcript variant 1
Gene name NUSAP1 (nucleolar and spindle associated protein 1)
Chromosome 15
Transcript - NCBI ID NM_016359.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_057443.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

81 entries on 1 page. Showing entries 1 - 81.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-49C>T r.(=) p.(=)
?/? c.-48G>C r.(=) p.(=)
?/? c.-27C>T r.(=) p.(=)
?/? c.-20C>T r.(=) p.(=)
?/? c.12C>T r.(=) p.(=)
?/? c.13T>A r.(?) p.(Ser5Thr)
?/? c.62C>T r.(?) p.(Ala21Val)
?/? c.93+31G>A r.(=) p.(=)
?/? c.94-19A>C r.(=) p.(=)
?/? c.94-17T>G r.(=) p.(=)
?/? c.97A>G r.(?) p.(Thr33Ala)
?/? c.98C>A r.(?) p.(Thr33Asn)
?/? c.128T>G r.(?) p.(Ile43Ser)
?/? c.162+8A>G r.(=) p.(=)
?/? c.162+37A>G r.(=) p.(=)
?/? c.163-28C>G r.(=) p.(=)
?/? c.287G>A r.(?) p.(Arg96His)
?/? c.299A>G r.(?) p.(Asp100Gly)
?/? c.302C>G r.(?) p.(Ser101*)
?/? c.306+48G>A r.(=) p.(=)
?/? c.307-37del r.(=) p.(=)
?/? c.307-31G>A r.(=) p.(=)
?/? c.307-27T>C r.(=) p.(=)
?/? c.307-3T>A r.spl? p.?
?/? c.313C>G r.(?) p.(His105Asp)
?/? c.341C>A r.(?) p.(Thr114Asn)
?/? c.351G>T r.(?) p.(Gln117His)
?/? c.390T>C r.(=) p.(=)
?/? c.401C>A r.(?) p.(Pro134His)
?/? c.440T>A r.(?) p.(Val147Asp)
?/? c.454A>G r.(?) p.(Arg152Gly)
?/? c.507A>G r.(=) p.(=)
?/? c.519del r.(?) p.(Asn175Ilefs*42)
?/? c.538A>G r.(?) p.(Ile180Val)
?/? c.550+47C>T r.(=) p.(=)
?/? c.551-14T>C r.(=) p.(=)
?/? c.560A>G r.(?) p.(Lys187Arg)
?/? c.571G>A r.(?) p.(Ala191Thr)
?/? c.590A>C r.(?) p.(Glu197Ala)
?/? c.689G>A r.(?) p.(Arg230Lys)
?/? c.735C>T r.(=) p.(=)
?/? c.744A>C r.(?) p.(Gln248His)
?/? c.745C>T r.(?) p.(Arg249*)
?/? c.746G>A r.(?) p.(Arg249Gln)
?/? c.749G>A r.(?) p.(Arg250His)
?/? c.753G>A r.(=) p.(=)
?/? c.760C>T r.(?) p.(Arg254Trp)
?/? c.789C>T r.(=) p.(=)
?/? c.816C>T r.(=) p.(=)
?/? c.848+38T>C r.(=) p.(=)
?/? c.849-39C>A r.(=) p.(=)
?/? c.849-6A>G r.(=) p.(=)
?/? c.849-4T>G r.spl? p.?
?/? c.860del r.(?) p.(Ala287Valfs*11)
?/? c.873T>C r.(=) p.(=)
?/? c.877C>T r.(?) p.(His293Tyr)
?/? c.878_879insT r.(?) p.(Lys294*)
?/? c.913T>A r.(?) p.(Ser305Thr)
?/? c.952G>A r.(?) p.(Glu318Lys)
?/? c.983C>T r.(?) p.(Thr328Ile)
?/? c.990G>A r.(=) p.(=)
?/? c.1001C>T r.(?) p.(Ala334Val)
?/? c.1006+25A>T r.(=) p.(=)
?/? c.1006+29_1006+30del r.(=) p.(=)
?/? c.1006+30G>T r.(=) p.(=)
?/? c.1041G>A r.(=) p.(=)
?/? c.1065A>G r.(=) p.(=)
?/? c.1109A>G r.(?) p.(Tyr370Cys)
?/? c.1123+47T>C r.(=) p.(=)
?/? c.1124-16C>T r.(=) p.(=)
?/? c.1199A>G r.(?) p.(Lys400Arg)
?/? c.1232+20G>T r.(=) p.(=)
?/? c.1233-35T>G r.(=) p.(=)
?/? c.1233-21T>C r.(=) p.(=)
?/? c.1233-11A>G r.(=) p.(=)
?/? c.1243C>T r.(?) p.(Arg415Trp)
?/? c.1253G>T r.(?) p.(Arg418Leu)
?/? c.1265G>A r.(?) p.(Arg422Gln)
?/? c.1303G>T r.(?) p.(Gly435Cys)
?/? c.1326A>G r.(=) p.(=)
?/? c.*36del r.(=) p.(=)
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