Transcript #00000078

Transcript name transcript variant 2
Gene name ABCF2 (ATP-binding cassette, sub-family F (GCN20), member 2)
Chromosome 7
Transcript - NCBI ID NM_005692.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_005683.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-17C>T r.(=) p.(=)
?/? c.9C>A r.(=) p.(=)
?/? c.12C>T r.(=) p.(=)
?/? c.13C>T r.(=) p.(=)
?/? c.154+45A>G r.(=) p.(=)
?/? c.154+46T>C r.(=) p.(=)
?/? c.154+52C>T r.(=) p.(=)
?/? c.155-46C>G r.(=) p.(=)
?/? c.155-37C>T r.(=) p.(=)
?/? c.155-27C>T r.(=) p.(=)
?/? c.155-4G>A r.spl? p.?
?/? c.159A>G r.(=) p.(=)
?/? c.186C>T r.(=) p.(=)
?/? c.245A>G r.(?) p.(Asn82Ser)
?/? c.279T>C r.(=) p.(=)
?/? c.335G>A r.(?) p.(Arg112His)
?/? c.338G>A r.(?) p.(Arg113His)
?/? c.368-47G>T r.(=) p.(=)
?/? c.368-39A>G r.(=) p.(=)
?/? c.389C>T r.(?) p.(Ala130Val)
?/? c.391A>G r.(?) p.(Ile131Val)
?/? c.409C>G r.(?) p.(Pro137Ala)
?/? c.426C>T r.(=) p.(=)
?/? c.532C>T r.(?) p.(Arg178Trp)
?/? c.533G>A r.(?) p.(Arg178Gln)
?/? c.550+11A>G r.(=) p.(=)
?/? c.551-36G>T r.(=) p.(=)
?/? c.551-35C>T r.(=) p.(=)
?/? c.551C>T r.(?) p.(Ala184Val)
?/? c.564G>A r.(=) p.(=)
?/? c.567C>T r.(=) p.(=)
?/? c.595C>T r.(=) p.(=)
?/? c.603C>T r.(=) p.(=)
?/? c.617T>C r.(?) p.(Met206Thr)
?/? c.628C>T r.(?) p.(Arg210Trp)
?/? c.651C>T r.(=) p.(=)
?/? c.667C>T r.(?) p.(Arg223Cys)
?/? c.668G>T r.(?) p.(Arg223Leu)
?/? c.671A>T r.(?) p.(Lys224Met)
?/? c.722+18T>C r.(=) p.(=)
?/? c.722+29A>G r.(=) p.(=)
?/? c.723-47A>G r.(=) p.(=)
?/? c.723-27G>A r.(=) p.(=)
?/? c.723-26C>T r.(=) p.(=)
?/? c.723-5T>C r.spl? p.?
?/? c.723-4del r.spl? p.?
?/? c.733A>T r.(?) p.(Ile245Phe)
?/? c.745A>G r.(?) p.(Met249Val)
?/? c.818+19G>C r.(=) p.(=)
?/? c.819-18G>C r.(=) p.(=)
?/? c.819-3C>T r.spl? p.?
?/? c.838C>G r.(?) p.(Leu280Val)
?/? c.879C>T r.(=) p.(=)
?/? c.921+18T>G r.(=) p.(=)
?/? c.921+31T>C r.(=) p.(=)
?/? c.921+43A>T r.(=) p.(=)
?/? c.921+45T>G r.(=) p.(=)
?/? c.921+47C>A r.(=) p.(=)
?/? c.922-13C>A r.(=) p.(=)
?/? c.922-11T>C r.(=) p.(=)
?/? c.925A>G r.(?) p.(Asn309Asp)
?/? c.939C>T r.(=) p.(=)
?/? c.950G>A r.(?) p.(Arg317Gln)
?/? c.1008A>T r.(=) p.(=)
?/? c.1017+33_1017+35del r.(=) p.(=)
?/? c.1018-39C>T r.(=) p.(=)
?/? c.1018-20C>T r.(=) p.(=)
?/? c.1018-14_1018-13del r.(=) p.(=)
?/? c.1029G>A r.(=) p.(=)
?/? c.1085C>T r.(?) p.(Thr362Met)
?/? c.1086G>A r.(=) p.(=)
?/? c.1098G>A r.(?) p.(Met366Ile)
?/? c.1125C>T r.(=) p.(=)
?/? c.1137+23G>A r.(=) p.(=)
?/? c.1137+29G>A r.(=) p.(=)
?/? c.1137+35G>A r.(=) p.(=)
?/? c.1137+23_1137+37del r.(=) p.(=)
?/? c.1138-18G>C r.(=) p.(=)
?/? c.1138-4C>T r.spl? p.?
?/? c.1190T>C r.(?) p.(Met397Thr)
?/? c.1227+27C>G r.(=) p.(=)
?/? c.1227+43G>A r.(=) p.(=)
?/? c.1228-16C>G r.(=) p.(=)
?/? c.1269C>T r.(=) p.(=)
?/? c.1293C>T r.(=) p.(=)
?/? c.1338+20G>C r.(=) p.(=)
?/? c.1339-39_1339-36del r.(=) p.(=)
?/? c.1339-22G>A r.(=) p.(=)
?/? c.1339-17T>C r.(=) p.(=)
?/? c.1391G>A r.(?) p.(Arg464His)
?/? c.1401+19del r.(=) p.(=)
?/? c.1401+39G>A r.(=) p.(=)
?/? c.1402-27C>G r.(=) p.(=)
?/? c.1402-4G>A r.spl? p.?
?/? c.1402-4_1402-3del r.spl? p.?
?/? c.1434A>G r.(=) p.(=)
?/? c.1470C>A r.(=) p.(=)
?/? c.1484A>C r.(?) p.(Glu495Ala)
?/? c.1498A>G r.(?) p.(Ile500Val)
?/? c.1499T>C r.(?) p.(Ile500Thr)
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