Transcript #00015808

Transcript name v-rel reticuloendotheliosis viral oncogene homolog (avian)
Gene name REL (v-rel reticuloendotheliosis viral oncogene homolog (avian))
Chromosome 2
Transcript - NCBI ID NM_002908.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_002899.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

89 entries on 1 page. Showing entries 1 - 89.
Legend  

Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-74_-71del r.(=) p.(=)
?/? c.-50C>G r.(=) p.(=)
?/? c.10+11A>T r.(=) p.(=)
?/? c.11-47T>G r.(=) p.(=)
?/? c.14C>T r.(?) p.(Ala5Val)
?/? c.15G>A r.(=) p.(=)
?/? c.24G>A r.(=) p.(=)
?/? c.29T>C r.(?) p.(Ile10Thr)
?/? c.49_78del r.(?) p.(Arg17_Lys26del)
?/? c.64C>T r.(?) p.(Arg22Cys)
?/? c.133C>A r.(=) p.(=)
?/? c.153+26T>C r.(=) p.(=)
?/? c.153+37G>A r.(=) p.(=)
?/? c.153+45A>T r.(=) p.(=)
?/? c.154-46A>C r.(=) p.(=)
?/? c.154-40G>A r.(=) p.(=)
?/? c.154-36A>G r.(=) p.(=)
?/? c.154-9T>A r.(=) p.(=)
?/? c.168T>C r.(=) p.(=)
?/? c.192A>G r.(=) p.(=)
?/? c.258C>T r.(=) p.(=)
?/? c.290G>A r.(?) p.(Arg97His)
?/? c.302+26C>T r.(=) p.(=)
?/? c.302+31_302+35del r.(=) p.(=)
?/? c.303-18T>C r.(=) p.(=)
?/? c.303-16_303-15insT r.(=) p.(=)
?/? c.394+28A>G r.(=) p.(=)
?/? c.394+50G>A r.(=) p.(=)
?/? c.395-25T>A r.(=) p.(=)
?/? c.395-18del r.(=) p.(=)
?/? c.395-18dup r.(=) p.(=)
?/? c.513C>T r.(=) p.(=)
?/? c.535+12A>G r.(=) p.(=)
?/? c.535+31_535+35del r.(=) p.(=)
?/? c.535+39_535+40insT r.(=) p.(=)
?/? c.535+48A>G r.(=) p.(=)
?/? c.564T>C r.(=) p.(=)
?/? c.584G>C r.(?) p.(Cys195Ser)
?/? c.641-49C>T r.(=) p.(=)
?/? c.754G>A r.(?) p.(Ala252Thr)
?/? c.767C>A r.(?) p.(Pro256His)
?/? c.854-29A>G r.(=) p.(=)
?/? c.854-3C>T r.spl? p.?
?/? c.866A>G r.(?) p.(Asn289Ser)
?/? c.921C>T r.(=) p.(=)
?/? c.922+18C>T r.(=) p.(=)
?/? c.923-38_923-37del r.(=) p.(=)
?/? c.972_973del r.(?) p.(Ser325Argfs*2)
?/? c.975_976del r.(?) p.(Gly326*)
?/? c.976_977del r.(?) p.(Gly326*)
?/? c.1019-45A>T r.(=) p.(=)
?/? c.1019-24A>C r.(=) p.(=)
?/? c.1034G>A r.(?) p.(Arg345Lys)
?/? c.1088-7C>A r.(=) p.(=)
?/? c.1100T>G r.(?) p.(Phe367Cys)
?/? c.1130C>G r.(?) p.(Pro377Arg)
?/? c.1131T>C r.(=) p.(=)
?/? c.1133C>T r.(?) p.(Thr378Ile)
?/? c.1160A>G r.(?) p.(Tyr387Cys)
?/? c.1161C>T r.(=) p.(=)
?/? c.1163A>G r.(?) p.(Tyr388Cys)
?/? c.1178C>G r.(?) p.(Pro393Arg)
?/? c.1210A>G r.(?) p.(Met404Val)
?/? c.1220T>C r.(?) p.(Leu407Pro)
?/? c.1222C>T r.(?) p.(Pro408Ser)
?/? c.1233C>G r.(?) p.(Ser411Arg)
?/? c.1271A>G r.(?) p.(Asn424Ser)
?/? c.1320G>A r.(=) p.(=)
?/? c.1390A>C r.(?) p.(Asn464His)
?/? c.1398C>T r.(=) p.(=)
?/? c.1399G>A r.(?) p.(Asp467Asn)
?/? c.1401T>C r.(=) p.(=)
?/? c.1410C>T r.(=) p.(=)
?/? c.1422G>A r.(=) p.(=)
?/? c.1442_1447del r.(?) p.(Leu482_Tyr483del)
?/? c.1448A>G r.(?) p.(Tyr483Cys)
?/? c.1462C>G r.(?) p.(Pro488Ala)
?/? c.1559A>G r.(?) p.(Glu520Gly)
?/? c.1605G>C r.(?) p.(Gln535His)
?/? c.1652A>G r.(?) p.(Asn551Ser)
?/? c.1659T>A r.(=) p.(=)
?/? c.1669T>C r.(?) p.(Ser557Pro)
?/? c.1674A>G r.(=) p.(=)
?/? c.1728T>C r.(=) p.(=)
?/? c.1734G>A r.(=) p.(=)
?/? c.1742C>T r.(?) p.(Ser581Leu)
?/? c.1769G>A r.(?) p.(Gly590Asp)
?/? c.1805G>A r.(?) p.(Ser602Asn)
?/? c.*40A>G r.(=) p.(=)
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