Transcript #00003338 (NM_138576.2, BCL11B gene)

Transcript name transcript variant 1
Gene name BCL11B (B-cell CLL/lymphoma 11B (zinc finger protein))
Chromosome 14
Transcript - NCBI ID NM_138576.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_612808.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

71 entries on 1 page. Showing entries 1 - 71.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_4_ c.(?_-854079)_(*587725_?)del r.0 p.0
+?/. - c.-0 r.0 p.0
+/. - c.0 r.0 p.0
+?/. - c.0 r.0 p.0
?/. - c.7C>A r.(?) p.(Arg3Ser)
?/. - c.38C>A r.(?) p.(Ser13Tyr)
-?/. - c.59-4C>G r.spl? p.?
-?/. - c.59-4C>G r.spl? p.?
-?/. - c.99C>T r.(?) p.(Asp33=)
+/. 2 c.211del r.(?) p.(Leu71TrpfsTer4)
-?/. - c.247G>A r.(?) p.(Gly83Ser)
-?/. - c.294G>A r.(?) p.(=)
+/. - c.400_403dup r.(?) p.(Cys135Tyrfs*61)
-?/. - c.427+5G>A r.spl? p.?
?/. - c.524G>T r.(?) p.(Gly175Val)
-?/. - c.543C>T r.(?) p.(Leu181=)
?/. - c.551C>G r.(?) p.(Pro184Arg)
-?/. - c.569C>T r.(?) p.(Pro190Leu)
-?/. - c.605C>T r.(?) p.(Thr202Met)
-/. - c.640+17C>T r.(=) p.(=)
?/. - c.738C>G r.(?) p.(Phe246Leu)
+?/. - c.747C>A r.(?) p.(Tyr249Ter)
-?/. - c.756C>T r.(?) p.(Pro252=)
+/. - c.781_808dup r.(?) p.(Gly270Alafs*256)
+?/. 4 c.785G>A r.(?) p.(Arg262Gln)
-?/. - c.919G>T r.(?) p.(Glu307*)
-?/. - c.933G>T r.(?) p.(Pro311=)
-?/. - c.1051C>T r.(?) p.(=)
+/. - c.1089del r.(?) p.(Ser364Argfs*29)
+/. - c.1259dup r.(?) p.(Gln421AlafsTer96)
?/. - c.1265C>T r.(?) p.(Pro422Leu)
+/. - c.1460_1485del r.(?) p.(Arg487Glnfs*21)
+?/. - c.1494dup r.(?) p.(Glu499ArgfsTer18)
?/. - c.1520G>A r.(?) p.(Gly507Asp)
-?/. - c.1560C>T r.(?) p.(His520=)
+?/. 4 c.1582del r.(?) p.(His528ThrfsTer35)
?/. - c.1602_1616dup r.(?) p.(Asp534_Glu538dup)
?/. - c.1617G>C r.(?) p.(Glu539Asp)
-?/. - c.1620G>C r.(?) p.(Glu540Asp)
-?/. - c.1624_1629del r.(?) p.(Glu542_Glu543del)
-/. - c.1627_1629del r.(?) p.(Glu543del)
-?/. - c.1627_1629dup r.(?) p.(Glu543dup)
-?/. - c.1633C>T r.(?) p.(Leu545=)
+?/. 4 c.1834G>T r.(?) p.(Glu612*)
+?/. - c.1887_1893del r.(?) p.(Gly630ThrfsTer91)
?/. - c.1892_1909dup r.(?) p.(Gly631_Asp636dup)
+/. - c.1916_1917dup r.(?) p.(Gly640ArgfsTer84)
+?/. - c.1933_1954del r.(?) p.(Ala645Thrfs*71)
-?/. - c.1935G>A r.(?) p.(Ala645=)
+?/. - c.1938_1965del r.(?) p.(Gly648AlafsTer66)
-?/. - c.1943G>T r.(?) p.(Gly648Val)
+/. - c.1943_1970del r.(?) p.(Gly648Alafs*66)
-?/. - c.1975G>A r.(?) p.(Ala659Thr)
?/. - c.2000G>A r.2000G>A p.Gly667Glu
?/. - c.2018C>G r.(?) p.(Pro673Arg)
+/. - c.2037del r.(?) p.(Leu681Serfs*42)
?/. - c.2038G>A r.(?) p.(Gly680Arg)
+?/. - c.2082_2107delinsCCA r.(?) p.(Glu695Hisfs*182)
?/. - c.2113G>A r.(?) p.(Glu705Lys)
?/. - c.2164A>G r.(?) p.(Met722Val)
?/. - c.2195C>T r.(?) p.(Ala732Val)
-?/. - c.2283C>T r.(?) p.(Asp761=)
+?/. 4 c.2421C>G r.(?) p.(Asn807Lys)
+/. - c.2438_2459del r.(?) p.(Val813Alafs*24)
+?/. 4 c.2439_2452dup r.(?) p.(His818ArgfsTer31)
+?/. 4 c.2439_2452dup r.(?) p.(His818ArgfsTer31)
+?/. 4 c.2448_2461del r.(?) p.(Ser817AlafsTer63)
+?/. - c.2519C>T r.(?) p.(Thr840Met)
?/. - c.2539G>A r.(?) p.(Gly847Arg)
?/. - c.*1048124G>A r.(=) p.(=)
?/. - c.*1091105A>G r.(=) p.(=)
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