Transcript #00001028

Transcript name AT rich interactive domain 3B (BRIGHT-like)
Gene name ARID3B (AT rich interactive domain 3B (BRIGHT-like))
Chromosome 15
Transcript - NCBI ID NM_006465.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_006456.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

81 entries on 1 page. Showing entries 1 - 81.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-52C>T r.(=) p.(=)
?/? c.13_15del r.(?) p.(Gln15del)
?/? c.13_15dup r.(?) p.(Gln15dup)
?/? c.37_39del r.(?) p.(Gln15del)
?/? c.39A>G r.(=) p.(=)
?/? c.49C>G r.(?) p.(Gln17Glu)
?/? c.135G>C r.(?) p.(Lys45Asn)
?/? c.150G>A r.(=) p.(=)
?/? c.178C>T r.(?) p.(Pro60Ser)
?/? c.198A>G r.(=) p.(=)
?/? c.203C>G r.(?) p.(Pro68Arg)
?/? c.225C>T r.(=) p.(=)
?/? c.247G>C r.(?) p.(Glu83Gln)
?/? c.251G>A r.(?) p.(Arg84Gln)
?/? c.254G>A r.(?) p.(Gly85Asp)
?/? c.280G>A r.(?) p.(Glu94Lys)
?/? c.285C>T r.(=) p.(=)
?/? c.286G>A r.(?) p.(Gly96Arg)
?/? c.301G>C r.(?) p.(Glu101Gln)
?/? c.319G>A r.(?) p.(Val107Ile)
?/? c.324A>G r.(=) p.(=)
?/? c.327G>A r.(=) p.(=)
?/? c.386G>A r.(?) p.(Arg129His)
?/? c.389A>G r.(?) p.(Gln130Arg)
?/? c.394C>G r.(?) p.(Pro132Ala)
?/? c.438C>T r.(=) p.(=)
?/? c.475A>G r.(?) p.(Lys159Glu)
?/? c.502G>C r.(?) p.(Val168Leu)
?/? c.537T>A r.(?) p.(Asp179Glu)
?/? c.552+17T>C r.(=) p.(=)
?/? c.553-4T>C r.spl? p.?
?/? c.592C>T r.(?) p.(Arg198Trp)
?/? c.624+30A>G r.(=) p.(=)
?/? c.624+30del r.(=) p.(=)
?/? c.624+48G>A r.(=) p.(=)
?/? c.625-64G>A r.(=) p.(=)
?/? c.625-33C>T r.(=) p.(=)
?/? c.625-19T>C r.(=) p.(=)
?/? c.679G>A r.(?) p.(Val227Ile)
?/? c.697+37A>G r.(=) p.(=)
?/? c.697+42G>A r.(=) p.(=)
?/? c.697+44T>C r.(=) p.(=)
?/? c.698-49C>A r.(=) p.(=)
?/? c.703C>T r.(?) p.(Pro235Ser)
?/? c.712C>A r.(=) p.(=)
?/? c.789G>A r.(=) p.(=)
?/? c.801C>G r.(?) p.(Asn267Lys)
?/? c.837C>T r.(=) p.(=)
?/? c.861C>T r.(=) p.(=)
?/? c.882-26C>G r.(=) p.(=)
?/? c.882-5T>C r.spl? p.?
?/? c.915G>A r.(=) p.(=)
?/? c.975G>A r.(=) p.(=)
?/? c.977G>A r.(?) p.(Gly326Asp)
?/? c.1005C>G r.(=) p.(=)
?/? c.1030_1031insCTGCTG r.(?) p.(Ala348_Ala349dup)
?/? c.1042G>A r.(?) p.(Ala348Thr)
?/? c.1082G>A r.(?) p.(Arg361His)
?/? c.1166-50T>G r.(=) p.(=)
?/? c.1166-33T>C r.(=) p.(=)
?/? c.1249C>G r.(?) p.(Arg417Gly)
?/? c.1258G>A r.(?) p.(Ala420Thr)
?/? c.1280G>A r.(?) p.(Arg427Gln)
?/? c.1312G>A r.(?) p.(Ala438Thr)
?/? c.1364G>A r.(?) p.(Arg455His)
?/? c.1381G>A r.(?) p.(Ala461Thr)
?/? c.1397T>C r.(?) p.(Met466Thr)
?/? c.1413C>T r.(=) p.(=)
?/? c.1420+15G>C r.(=) p.(=)
?/? c.1420+39A>G r.(=) p.(=)
?/? c.1421-30C>T r.(=) p.(=)
?/? c.1463C>T r.(?) p.(Thr488Met)
?/? c.1486A>G r.(?) p.(Met496Val)
?/? c.1519+31C>T r.(=) p.(=)
?/? c.1519+38G>A r.(=) p.(=)
?/? c.1520-42G>A r.(=) p.(=)
?/? c.1527G>A r.(=) p.(=)
?/? c.1592_1593insCAG r.(?) p.(Ser537dup)
?/? c.1608C>T r.(=) p.(=)
?/? c.1653C>T r.(=) p.(=)
?/? c.*5C>T r.(=) p.(=)
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