Transcript #00011844

Transcript name transcript variant 1
Gene name MKI67 (antigen identified by monoclonal antibody Ki-67)
Chromosome 10
Transcript - NCBI ID NM_002417.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_002408.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

496 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-15C>T r.(=) p.(=)
?/? c.-7T>G r.(=) p.(=)
?/? c.-3A>T r.(=) p.(=)
?/? c.4T>C r.(?) p.(Trp2Arg)
?/? c.85T>C r.(?) p.(Phe29Leu)
?/? c.93-21_93-20insA r.(=) p.(=)
?/? c.93-6A>G r.(=) p.(=)
?/? c.171+32A>C r.(=) p.(=)
?/? c.171+40A>C r.(=) p.(=)
?/? c.172-35A>G r.(=) p.(=)
?/? c.172-25T>C r.(=) p.(=)
?/? c.196A>G r.(?) p.(Thr66Ala)
?/? c.237T>A r.(=) p.(=)
?/? c.267T>A r.(=) p.(=)
?/? c.287+19G>T r.(=) p.(=)
?/? c.288-53C>T r.(=) p.(=)
?/? c.288-41T>C r.(=) p.(=)
?/? c.310A>C r.(?) p.(Asn104His)
?/? c.311A>G r.(?) p.(Asn104Ser)
?/? c.318G>A r.(=) p.(=)
?/? c.354G>A r.(=) p.(=)
?/? c.354+27del r.(=) p.(=)
?/? c.364C>T r.(?) p.(Arg122Cys)
?/? c.368G>A r.(?) p.(Arg123His)
?/? c.397C>T r.(?) p.(Pro133Ser)
?/? c.400+4A>G r.spl? p.?
?/? c.400+6T>C r.(=) p.(=)
?/? c.400+25C>T r.(=) p.(=)
?/? c.400+44G>A r.(=) p.(=)
?/? c.401-16A>G r.(=) p.(=)
?/? c.473A>G r.(?) p.(His158Arg)
?/? c.488A>G r.(?) p.(Lys163Arg)
?/? c.501C>T r.(=) p.(=)
?/? c.510C>G r.(?) p.(Asp170Glu)
?/? c.521G>T r.(?) p.(Ser174Ile)
?/? c.544G>A r.(?) p.(Val182Ile)
?/? c.595A>G r.(?) p.(Ile199Val)
?/? c.623G>A r.(?) p.(Ser208Asn)
?/? c.625G>A r.(?) p.(Val209Ile)
?/? c.647G>A r.(?) p.(Gly216Glu)
?/? c.648A>T r.(=) p.(=)
?/? c.671C>T r.(?) p.(Thr224Ile)
?/? c.673C>T r.(?) p.(Gln225*)
?/? c.712T>A r.(?) p.(Trp238Arg)
?/? c.730G>A r.(?) p.(Val244Met)
?/? c.763G>A r.(?) p.(Glu255Lys)
?/? c.794G>T r.(?) p.(Gly265Val)
?/? c.795A>T r.(=) p.(=)
?/? c.811G>A r.(?) p.(Ala271Thr)
?/? c.814A>T r.(?) p.(Thr272Ser)
?/? c.840A>G r.(=) p.(=)
?/? c.866C>T r.(?) p.(Ser289Leu)
?/? c.867G>A r.(=) p.(=)
?/? c.868C>T r.(?) p.(Arg290Cys)
?/? c.869G>A r.(?) p.(Arg290His)
?/? c.895A>C r.(?) p.(Ser299Arg)
?/? c.945G>T r.(?) p.(Gln315His)
?/? c.957G>T r.(?) p.(Lys319Asn)
?/? c.967G>A r.(?) p.(Val323Met)
?/? c.1003G>A r.(?) p.(Ala335Thr)
?/? c.1016T>G r.(?) p.(Leu339Arg)
?/? c.1022A>T r.(?) p.(Glu341Val)
?/? c.1042C>A r.(?) p.(Pro348Thr)
?/? c.1140T>G r.(?) p.(Ser380Arg)
?/? c.1147T>C r.(?) p.(Phe383Leu)
?/? c.1175C>T r.(?) p.(Pro392Leu)
?/? c.1182G>A r.(=) p.(=)
?/? c.1198C>T r.(?) p.(Arg400*)
?/? c.1224A>C r.(=) p.(=)
?/? c.1246G>T r.(?) p.(Glu416*)
?/? c.1254C>G r.(=) p.(=)
?/? c.1255T>C r.(?) p.(Ser419Pro)
?/? c.1299G>A r.(=) p.(=)
?/? c.1304C>T r.(?) p.(Thr435Met)
?/? c.1305G>A r.(=) p.(=)
?/? c.1318C>T r.(?) p.(His440Tyr)
?/? c.1342_1343del r.(?) p.(Trp448Alafs*5)
?/? c.1349C>T r.(?) p.(Thr450Ile)
?/? c.1469G>T r.(?) p.(Gly490Val)
?/? c.1480+1G>A r.spl? p.?
?/? c.1481-33T>C r.(=) p.(=)
?/? c.1481-28C>G r.(=) p.(=)
?/? c.1481-12C>T r.(=) p.(=)
?/? c.1481-11C>T r.(=) p.(=)
?/? c.1481-3T>C r.spl? p.?
?/? c.1482T>A r.(?) p.(Asn494Lys)
?/? c.1491G>C r.(?) p.(Glu497Asp)
?/? c.1513C>T r.(?) p.(Arg505Cys)
?/? c.1539A>T r.(?) p.(Arg513Ser)
?/? c.1574C>T r.(?) p.(Thr525Met)
?/? c.1598C>T r.(?) p.(Pro533Leu)
?/? c.1603A>G r.(?) p.(Lys535Glu)
?/? c.1604A>G r.(?) p.(Lys535Arg)
?/? c.1622T>A r.(?) p.(Met541Lys)
?/? c.1624C>G r.(?) p.(His542Asp)
?/? c.1628C>G r.(?) p.(Thr543Ser)
?/? c.1667A>C r.(?) p.(Gln556Pro)
?/? c.1668A>T r.(?) p.(Gln556His)
?/? c.1691G>T r.(?) p.(Gly564Val)
?/? c.1724G>A r.(?) p.(Ser575Asn)
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