Transcript #00001529 (NM_014739.2, BCLAF1 gene)

Transcript name transcript variant 1
Gene name BCLAF1 (BCL2-associated transcription factor 1)
Chromosome 6
Transcript - NCBI ID NM_014739.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_055554.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.8G>A r.(?) p.(Arg3His)
?/? c.25C>T r.(?) p.(His9Tyr)
?/? c.26A>G r.(?) p.(His9Arg)
?/? c.97C>T r.(?) p.(Arg33*)
?/? c.105-15T>G r.(=) p.(=)
?/? c.139C>T r.(?) p.(Arg47Cys)
?/? c.140G>A r.(?) p.(Arg47His)
?/? c.152G>A r.(?) p.(Arg51His)
?/? c.238T>C r.(?) p.(Tyr80His)
?/? c.244C>G r.(?) p.(Gln82Glu)
?/? c.269G>A r.(?) p.(Arg90Gln)
?/? c.284C>T r.(?) p.(Pro95Leu)
?/? c.296G>C r.(?) p.(Arg99Thr)
?/? c.305C>T r.(?) p.(Ser102Phe)
?/? c.307A>C r.(=) p.(=)
?/? c.319C>T r.(?) p.(Arg107*)
?/? c.320G>A r.(?) p.(Arg107Gln)
?/? c.325C>T r.(?) p.(Arg109Cys)
?/? c.332G>A r.(?) p.(Arg111His)
?/? c.357C>T r.(=) p.(=)
?/? c.389G>A r.(?) p.(Arg130His)
?/? c.391C>T r.(?) p.(Arg131Trp)
?/? c.392G>A r.(?) p.(Arg131Gln)
?/? c.393G>A r.(=) p.(=)
?/? c.399T>C r.(=) p.(=)
?/? c.401G>T r.(?) p.(Arg134Ile)
?/? c.433C>T r.(?) p.(Arg145Cys)
?/? c.434G>A r.(?) p.(Arg145His)
?/? c.454A>T r.(?) p.(Lys152*)
?/? c.475C>T r.(?) p.(Arg159*)
?/? c.479_480insAGG r.(?) p.(Gly160dup)
?/? c.495A>T r.(?) p.(Gln165His)
?/? c.530G>A r.(?) p.(Ser177Asn)
?/? c.534G>A r.(=) p.(=)
?/? c.560C>A r.(?) p.(Pro187Gln)
?/? c.561G>A r.(=) p.(=)
?/? c.628G>A r.(?) p.(Gly210Ser)
?/? c.629G>A r.(?) p.(Gly210Asp)
?/? c.640C>T r.(?) p.(Pro214Ser)
?/? c.682A>C r.(?) p.(Ser228Arg)
?/? c.694A>G r.(?) p.(Ile232Val)
?/? c.734C>T r.(?) p.(Ala245Val)
?/? c.744C>T r.(=) p.(=)
?/? c.749C>G r.(?) p.(Thr250Arg)
?/? c.751G>T r.(?) p.(Val251Phe)
?/? c.786A>T r.(=) p.(=)
?/? c.800A>G r.(?) p.(His267Arg)
?/? c.811A>G r.(?) p.(Arg271Gly)
?/? c.829G>A r.(?) p.(Val277Ile)
?/? c.842C>G r.(?) p.(Ser281Cys)
?/? c.848G>A r.(?) p.(Arg283Gln)
?/? c.856C>T r.(?) p.(Pro286Ser)
?/? c.892C>T r.(?) p.(Arg298*)
?/? c.893G>A r.(?) p.(Arg298Gln)
?/? c.895A>G r.(?) p.(Arg299Gly)
?/? c.910A>T r.(?) p.(Thr304Ser)
?/? c.913A>G r.(?) p.(Ile305Val)
?/? c.921A>G r.(=) p.(=)
?/? c.940G>A r.(?) p.(Glu314Lys)
?/? c.952C>T r.(?) p.(Arg318Cys)
?/? c.953G>A r.(?) p.(Arg318His)
?/? c.959C>T r.(?) p.(Ser320Leu)
?/? c.982C>A r.(?) p.(Gln328Lys)
?/? c.1016+9_1016+10insTTTT r.(=) p.(=)
?/? c.1016+35T>C r.(=) p.(=)
?/? c.1017-24A>G r.(=) p.(=)
?/? c.1017-21C>G r.(=) p.(=)
?/? c.1064C>T r.(?) p.(Thr355Ile)
?/? c.1150T>C r.(?) p.(Phe384Leu)
?/? c.1153A>G r.(?) p.(Ser385Gly)
?/? c.1160_1161del r.(?) p.(Lys387Argfs*8)
?/? c.1181T>C r.(?) p.(Phe394Ser)
?/? c.1185T>C r.(=) p.(=)
?/? c.1207G>T r.(?) p.(Glu403*)
?/? c.1214C>G r.(?) p.(Thr405Arg)
?/? c.1242A>C r.(=) p.(=)
?/? c.1252G>C r.(?) p.(Asp418His)
?/? c.1273A>G r.(?) p.(Thr425Ala)
?/? c.1274C>T r.(?) p.(Thr425Ile)
?/? c.1285C>T r.(?) p.(Arg429Trp)
?/? c.1286G>A r.(?) p.(Arg429Gln)
?/? c.1294G>A r.(?) p.(Glu432Lys)
?/? c.1337G>A r.(?) p.(Gly446Asp)
?/? c.1353T>C r.(=) p.(=)
?/? c.1399G>A r.(?) p.(Val467Ile)
?/? c.1407A>T r.(?) p.(Glu469Asp)
?/? c.1432C>T r.(?) p.(His478Tyr)
?/? c.1489C>T r.(?) p.(Pro497Ser)
?/? c.1493A>C r.(?) p.(Glu498Ala)
?/? c.1546C>A r.(?) p.(His516Asn)
?/? c.1556T>C r.(?) p.(Leu519Pro)
?/? c.1564C>T r.(?) p.(Arg522*)
?/? c.1575T>C r.(=) p.(=)
?/? c.1577C>T r.(?) p.(Thr526Ile)
?/? c.1582A>C r.(=) p.(=)
?/? c.1616C>T r.(?) p.(Ala539Val)
?/? c.1617G>A r.(=) p.(=)
?/? c.1621G>A r.(?) p.(Asp541Asn)
?/? c.1630C>T r.(?) p.(Arg544Cys)
?/? c.1631G>A r.(?) p.(Arg544His)
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