Transcript #00001433 (NM_021813.2, BACH2 gene)

Transcript name transcript variant 1
Gene name BACH2 (BTB and CNC homology 1, basic leucine zipper transcription factor 2)
Chromosome 6
Transcript - NCBI ID NM_021813.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_068585.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.15G>A r.(=) p.(=)
?/? c.134G>A r.(?) p.(Arg45Lys)
?/? c.162G>T r.(=) p.(=)
?/? c.168C>T r.(=) p.(=)
?/? c.195G>T r.(=) p.(=)
?/? c.243+40del r.(=) p.(=)
?/? c.243+40A>G r.(=) p.(=)
?/? c.243+49C>G r.(=) p.(=)
?/? c.244-29T>C r.(=) p.(=)
?/? c.249A>G r.(=) p.(=)
?/? c.330C>T r.(=) p.(=)
?/? c.332G>A r.(?) p.(Arg111His)
?/? c.381C>T r.(=) p.(=)
?/? c.431G>A r.(?) p.(Arg144Gln)
?/? c.444G>A r.(=) p.(=)
?/? c.452G>C r.(?) p.(Arg151Pro)
?/? c.468C>T r.(=) p.(=)
?/? c.469G>A r.(?) p.(Glu157Lys)
?/? c.530A>G r.(?) p.(Lys177Arg)
?/? c.583G>A r.(?) p.(Ala195Thr)
?/? c.677C>T r.(?) p.(Thr226Met)
?/? c.729T>C r.(=) p.(=)
?/? c.744C>T r.(=) p.(=)
?/? c.746G>C r.(?) p.(Ser249Thr)
?/? c.773G>A r.(?) p.(Arg258Gln)
?/? c.796C>T r.(?) p.(Leu266Phe)
?/? c.822G>A r.(=) p.(=)
?/? c.838C>A r.(?) p.(Pro280Thr)
?/? c.847G>A r.(?) p.(Glu283Lys)
?/? c.863G>A r.(?) p.(Ser288Asn)
?/? c.871C>G r.(?) p.(Leu291Val)
?/? c.931C>T r.(?) p.(Arg311Trp)
?/? c.962C>T r.(?) p.(Thr321Met)
?/? c.981_982insCCCC r.(?) p.(Cys328Profs*47)
?/? c.1004T>C r.(?) p.(Val335Ala)
?/? c.1018T>A r.(?) p.(Cys340Ser)
?/? c.1020C>T r.(=) p.(=)
?/? c.1071C>T r.(=) p.(=)
?/? c.1219A>T r.(?) p.(Met407Leu)
?/? c.1227G>C r.(=) p.(=)
?/? c.1244G>A r.(?) p.(Gly415Glu)
?/? c.1252G>A r.(?) p.(Ala418Thr)
?/? c.1259G>C r.(?) p.(Cys420Ser)
?/? c.1308C>T r.(=) p.(=)
?/? c.1309G>A r.(?) p.(Ala437Thr)
?/? c.1320A>T r.(?) p.(Gln440His)
?/? c.1325G>A r.(?) p.(Ser442Asn)
?/? c.1364A>G r.(?) p.(Asp455Gly)
?/? c.1382C>T r.(?) p.(Pro461Leu)
?/? c.1427G>T r.(?) p.(Ser476Ile)
?/? c.1435G>A r.(?) p.(Ala479Thr)
?/? c.1446C>T r.(=) p.(=)
?/? c.1447G>A r.(?) p.(Gly483Ser)
?/? c.1475G>T r.(?) p.(Gly492Val)
?/? c.1503G>A r.(=) p.(=)
?/? c.1506A>G r.(=) p.(=)
?/? c.1514A>G r.(?) p.(Lys505Arg)
?/? c.1536C>G r.(=) p.(=)
?/? c.1560C>G r.(=) p.(=)
?/? c.1601G>A r.(?) p.(Gly534Glu)
?/? c.1603G>A r.(?) p.(Gly535Ser)
?/? c.1656G>T r.(?) p.(Gln552His)
?/? c.1735A>G r.(?) p.(Ile579Val)
?/? c.1743T>G r.(?) p.(Cys581Trp)
?/? c.1779C>T r.(=) p.(=)
?/? c.1806G>A r.(=) p.(=)
?/? c.1837-39C>T r.(=) p.(=)
?/? c.1921T>G r.(?) p.(Ser641Ala)
?/? c.1943A>G r.(?) p.(His648Arg)
?/? c.1944T>C r.(=) p.(=)
?/? c.1980C>T r.(=) p.(=)
?/? c.2043+32C>G r.(=) p.(=)
?/? c.2043+33T>C r.(=) p.(=)
?/? c.2044-11C>T r.(=) p.(=)
?/? c.2044-7T>C r.(=) p.(=)
?/? c.2103A>G r.(=) p.(=)
?/? c.2160C>T r.(=) p.(=)
?/? c.2183G>A r.(?) p.(Arg728Gln)
?/? c.2191C>T r.(?) p.(Pro731Ser)
?/? c.2207T>C r.(?) p.(Met736Thr)
?/? c.2220G>A r.(=) p.(=)
?/? c.2240C>T r.(?) p.(Ala747Val)
?/? c.2241G>A r.(=) p.(=)
?/? c.2280C>T r.(=) p.(=)
?/? c.2281G>A r.(?) p.(Ala761Thr)
?/? c.2295C>T r.(=) p.(=)
?/? c.2299C>T r.(?) p.(Pro767Ser)
?/? c.2310G>A r.(=) p.(=)
?/? c.2315C>T r.(?) p.(Pro772Leu)
?/? c.2319C>T r.(=) p.(=)
?/? c.2321C>T r.(?) p.(Ala774Val)
?/? c.2322G>A r.(=) p.(=)
?/? c.2326C>A r.(?) p.(Pro776Thr)
?/? c.2327C>T r.(?) p.(Pro776Leu)
?/? c.2331C>T r.(=) p.(=)
?/? c.2337C>A r.(=) p.(=)
?/? c.2361C>T r.(=) p.(=)
?/? c.2386C>T r.(=) p.(=)
?/? c.2402C>T r.(?) p.(Pro801Leu)
?/? c.2403G>A r.(=) p.(=)
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