Transcript #00004993

Transcript name transcript variant a
Gene name DYRK1B (dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B)
Chromosome 19
Transcript - NCBI ID NM_004714.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_004705.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.21T>C r.(=) p.(=)
?/? c.60G>T r.(=) p.(=)
?/? c.63+15G>C r.(=) p.(=)
?/? c.63+38G>T r.(=) p.(=)
?/? c.64-24C>T r.(=) p.(=)
?/? c.79C>T r.(?) p.(Arg27Trp)
?/? c.80G>A r.(?) p.(Arg27Gln)
?/? c.83T>C r.(?) p.(Leu28Pro)
?/? c.106G>C r.(?) p.(Ala36Pro)
?/? c.132G>A r.(=) p.(=)
?/? c.165C>T r.(=) p.(=)
?/? c.183+40G>T r.(=) p.(=)
?/? c.194C>T r.(?) p.(Ala65Val)
?/? c.202A>C r.(?) p.(Lys68Gln)
?/? c.209G>A r.(?) p.(Arg70Gln)
?/? c.210G>A r.(=) p.(=)
?/? c.230A>G r.(?) p.(Gln77Arg)
?/? c.263T>C r.(?) p.(Leu88Pro)
?/? c.282C>T r.(=) p.(=)
?/? c.283G>A r.(?) p.(Asp95Asn)
?/? c.291T>C r.(=) p.(=)
?/? c.300C>T r.(=) p.(=)
?/? c.304C>T r.(?) p.(Arg102Cys)
?/? c.305G>A r.(?) p.(Arg102His)
?/? c.313G>A r.(?) p.(Glu105Lys)
?/? c.373-45G>C r.(=) p.(=)
?/? c.373-10G>T r.(=) p.(=)
?/? c.373-7C>T r.(=) p.(=)
?/? c.520+25G>A r.(=) p.(=)
?/? c.520+36G>A r.(=) p.(=)
?/? c.521-37G>A r.(=) p.(=)
?/? c.521-9C>T r.(=) p.(=)
?/? c.521-4G>A r.spl? p.?
?/? c.562C>T r.(=) p.(=)
?/? c.591G>A r.(=) p.(=)
?/? c.594C>T r.(=) p.(=)
?/? c.619C>T r.(?) p.(Arg207Cys)
?/? c.621C>T r.(=) p.(=)
?/? c.656A>G r.(?) p.(Gln219Arg)
?/? c.668C>T r.(?) p.(Thr223Met)
?/? c.690G>A r.(=) p.(=)
?/? c.780C>T r.(=) p.(=)
?/? c.781G>A r.(?) p.(Gly261Ser)
?/? c.807+9C>T r.(=) p.(=)
?/? c.808-24C>G r.(=) p.(=)
?/? c.870C>T r.(=) p.(=)
?/? c.871G>A r.(?) p.(Asp291Asn)
?/? c.875del r.(?) p.(Leu292Argfs*31)
?/? c.954+12G>A r.(=) p.(=)
?/? c.954+16G>C r.(=) p.(=)
?/? c.954+18G>A r.(=) p.(=)
?/? c.955-22C>T r.(=) p.(=)
?/? c.955-21T>C r.(=) p.(=)
?/? c.955-15C>T r.(=) p.(=)
?/? c.955-3C>T r.spl? p.?
?/? c.1002C>T r.(=) p.(=)
?/? c.1007T>C r.(?) p.(Met336Thr)
?/? c.1030C>T r.(?) p.(Arg344Cys)
?/? c.1031G>A r.(?) p.(Arg344His)
?/? c.1055G>C r.(?) p.(Gly352Ala)
?/? c.1086A>T r.(?) p.(Glu362Asp)
?/? c.1095+32C>T r.(=) p.(=)
?/? c.1095+35C>T r.(=) p.(=)
?/? c.1095+36G>A r.(=) p.(=)
?/? c.1201del r.(?) p.(Tyr401Thrfs*102)
?/? c.1205_1206insGCC r.(?) p.(Leu402_Arg403insPro)
?/? c.1252G>A r.(?) p.(Ala418Thr)
?/? c.1284C>T r.(=) p.(=)
?/? c.1287C>T r.(=) p.(=)
?/? c.1302G>A r.(=) p.(=)
?/? c.1315A>G r.(?) p.(Thr439Ala)
?/? c.1320C>T r.(=) p.(=)
?/? c.1324G>C r.(?) p.(Gly442Arg)
?/? c.1336A>G r.(?) p.(Ser446Gly)
?/? c.1359G>A r.(=) p.(=)
?/? c.1411+32C>T r.(=) p.(=)
?/? c.1411+41del r.(=) p.(=)
?/? c.1412-23C>T r.(=) p.(=)
?/? c.1442G>A r.(?) p.(Arg481Gln)
?/? c.1451G>A r.(?) p.(Arg484His)
?/? c.1467T>C r.(=) p.(=)
?/? c.1474G>A r.(?) p.(Gly492Ser)
?/? c.1484C>T r.(?) p.(Pro495Leu)
?/? c.1492A>G r.(?) p.(Thr498Ala)
?/? c.1503G>A r.(=) p.(=)
?/? c.1518+26G>A r.(=) p.(=)
?/? c.1518+29G>C r.(=) p.(=)
?/? c.1519-28A>G r.(=) p.(=)
?/? c.1519-26C>T r.(=) p.(=)
?/? c.1521C>T r.(=) p.(=)
?/? c.1526C>T r.(?) p.(Pro509Leu)
?/? c.1586C>A r.(?) p.(Pro529His)
?/? c.1598C>T r.(?) p.(Ser533Leu)
?/? c.1613C>G r.(?) p.(Thr538Ser)
?/? c.1640G>A r.(?) p.(Arg547Gln)
?/? c.1652G>A r.(?) p.(Arg551His)
?/? c.1683G>A r.(=) p.(=)
?/? c.1732C>T r.(?) p.(Pro578Ser)
?/? c.1733C>T r.(?) p.(Pro578Leu)
?/? c.1777C>T r.(?) p.(Arg593Trp)
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