Transcript #00013874

Transcript name poly (ADP-ribose) polymerase family, member 14
Gene name PARP14 (poly (ADP-ribose) polymerase family, member 14)
Chromosome 3
Transcript - NCBI ID NM_017554.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_060024.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-46C>A r.(=) p.(=)
?/? c.-16G>C r.(=) p.(=)
?/? c.16T>G r.(?) p.(Ser6Ala)
?/? c.169_171del r.(?) p.(Phe58del)
?/? c.185A>C r.(?) p.(Asp62Ala)
?/? c.188-46A>G r.(=) p.(=)
?/? c.188-22T>C r.(=) p.(=)
?/? c.288C>T r.(=) p.(=)
?/? c.321+1G>A r.spl? p.?
?/? c.321+35A>T r.(=) p.(=)
?/? c.321+37G>T r.(=) p.(=)
?/? c.321+49G>A r.(=) p.(=)
?/? c.322-62A>T r.(=) p.(=)
?/? c.322-13G>A r.(=) p.(=)
?/? c.322-7G>A r.(=) p.(=)
?/? c.355+3A>G r.spl? p.?
?/? c.355+68G>A r.(=) p.(=)
?/? c.356-27G>T r.(=) p.(=)
?/? c.356-4T>C r.spl? p.?
?/? c.394G>A r.(?) p.(Gly132Ser)
?/? c.598+40A>G r.(=) p.(=)
?/? c.599-20_599-19del r.(=) p.(=)
?/? c.599-19del r.(=) p.(=)
?/? c.599-19dup r.(=) p.(=)
?/? c.635A>G r.(?) p.(His212Arg)
?/? c.688A>G r.(?) p.(Ile230Val)
?/? c.703C>G r.(?) p.(Leu235Val)
?/? c.829A>C r.(=) p.(=)
?/? c.836-46C>A r.(=) p.(=)
?/? c.836-8C>G r.(=) p.(=)
?/? c.837G>A r.(=) p.(=)
?/? c.855C>T r.(=) p.(=)
?/? c.864C>T r.(=) p.(=)
?/? c.1035C>T r.(=) p.(=)
?/? c.1036G>A r.(?) p.(Asp346Asn)
?/? c.1133C>T r.(?) p.(Pro378Leu)
?/? c.1185G>A r.(=) p.(=)
?/? c.1223C>A r.(?) p.(Thr408Lys)
?/? c.1244A>G r.(?) p.(Asn415Ser)
?/? c.1248T>G r.(?) p.(Asp416Glu)
?/? c.1333A>C r.(?) p.(Ile445Leu)
?/? c.1342C>G r.(?) p.(Gln448Glu)
?/? c.1349G>A r.(?) p.(Arg450Lys)
?/? c.1459C>T r.(=) p.(=)
?/? c.1462G>A r.(?) p.(Asp488Asn)
?/? c.1473C>T r.(=) p.(=)
?/? c.1475C>T r.(?) p.(Thr492Met)
?/? c.1476G>A r.(=) p.(=)
?/? c.1479G>A r.(=) p.(=)
?/? c.1511T>A r.(?) p.(Val504Asp)
?/? c.1560A>G r.(=) p.(=)
?/? c.1572C>T r.(=) p.(=)
?/? c.1599G>A r.(=) p.(=)
?/? c.1640A>G r.(?) p.(Gln547Arg)
?/? c.1682C>A r.(?) p.(Ala561Glu)
?/? c.1703A>G r.(?) p.(Tyr568Cys)
?/? c.1734C>G r.(=) p.(=)
?/? c.1750G>A r.(?) p.(Ala584Thr)
?/? c.1835A>G r.(?) p.(Lys612Arg)
?/? c.1890C>A r.(?) p.(Asn630Lys)
?/? c.1891A>G r.(?) p.(Thr631Ala)
?/? c.1993G>A r.(?) p.(Val665Ile)
?/? c.2097G>T r.(?) p.(Lys699Asn)
?/? c.2108A>G r.(?) p.(Gln703Arg)
?/? c.2149C>T r.(=) p.(=)
?/? c.2167G>A r.(?) p.(Glu723Lys)
?/? c.2183T>A r.(?) p.(Val728Glu)
?/? c.2197C>A r.(?) p.(Gln733Lys)
?/? c.2216G>A r.(?) p.(Cys739Tyr)
?/? c.2285A>G r.(?) p.(Gln762Arg)
?/? c.2299C>T r.(?) p.(Arg767Trp)
?/? c.2362G>A r.(?) p.(Ala788Thr)
?/? c.2383C>T r.(?) p.(Arg795Trp)
?/? c.2437C>T r.(?) p.(Arg813Trp)
?/? c.2448C>T r.(=) p.(=)
?/? c.2490T>C r.(=) p.(=)
?/? c.2553G>C r.(?) p.(Gln851His)
?/? c.2582C>G r.(?) p.(Pro861Arg)
?/? c.2592C>T r.(=) p.(=)
?/? c.2607A>T r.(=) p.(=)
?/? c.2628C>T r.(=) p.(=)
?/? c.2639C>A r.(?) p.(Ala880Glu)
?/? c.2649C>T r.(=) p.(=)
?/? c.2659G>C r.(?) p.(Gly887Arg)
?/? c.2673G>A r.(=) p.(=)
?/? c.2695A>G r.(?) p.(Arg899Gly)
?/? c.2795G>A r.(?) p.(Arg932Gln)
?/? c.2799C>T r.(=) p.(=)
?/? c.2800G>A r.(?) p.(Val934Met)
?/? c.2830A>T r.(?) p.(Asn944Tyr)
?/? c.2877T>C r.(=) p.(=)
?/? c.2899G>A r.(?) p.(Val967Ile)
?/? c.2905G>A r.(?) p.(Ala969Thr)
?/? c.2977C>T r.(?) p.(Pro993Ser)
?/? c.3021C>T r.(=) p.(=)
?/? c.3081+10G>A r.(=) p.(=)
?/? c.3082-15G>C r.(=) p.(=)
?/? c.3084C>T r.(=) p.(=)
?/? c.3085G>T r.(?) p.(Asp1029Tyr)
?/? c.3166C>T r.(?) p.(Pro1056Ser)
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