Transcript #00014309 (NM_015909.3, NBAS gene)

Transcript name transcript variant 1
Gene name NBAS (neuroblastoma amplified sequence)
Chromosome 2
Transcript - NCBI ID NM_015909.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_056993.2
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

318 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.1A>G r.(?) p.(Met1?)
+/. 1i c.118-2A>G r.spl p.?
-/. - c.130C>G r.(?) p.(Gln44Glu)
-?/. - c.130C>G r.(?) p.(Gln44Glu)
-?/. - c.172+4A>C r.spl? p.?
-?/. - c.219T>C r.(?) p.(Pro73=)
-/. - c.287+9G>C r.(=) p.(=)
-/. - c.287+20_287+21insT r.(=) p.(=)
-/. - c.287+20_287+21insT r.(=) p.(=)
?/. - c.320A>G r.(?) p.(Gln107Arg)
?/. - c.335+4A>G r.spl? p.?
+/. - c.409C>T r.409c>u p.Arg137Trp
-?/. - c.450C>T r.(?) p.(Ala150=)
-?/. - c.450C>T r.(?) p.(Ala150=)
-?/. - c.450C>T r.(?) p.(Ala150=)
-/. - c.514-11C>T r.(=) p.(=)
-/. - c.514-11C>T r.(=) p.(=)
-?/. - c.540C>T r.(?) p.(Ser180=)
-?/. - c.540C>T r.(?) p.(Ser180=)
+/. 8 c.558_560del r.(?) p.(Ile187del)
+/. 8 c.603_605del r.(?) p.(Leu202del)
?/. - c.607G>C r.(?) p.(Val203Leu)
-/. - c.648-14C>T r.(=) p.(=)
-?/. - c.648-7A>T r.(=) p.(=)
-?/. - c.648-7A>T r.(=) p.(=)
?/. - c.656C>G r.(?) p.(Thr219Arg)
-?/. - c.672A>G r.(?) p.(Gln224=)
+/. 9 c.686dup r.(?) p.(Ser230Glnfs*4)
+/. 9 c.686dup r.(?) p.(Ser230Glnfs*4)
+/. 9 c.686dup r.(?) p.(Ser230Glnfs*4)
+/. - c.686dup r.(?) p.(Ser230Glnfs*4)
-/. - c.711T>C r.(?) p.(His237=)
-?/. - c.711T>C r.(?) p.(His237=)
-?/. - c.711T>C r.(?) p.(His237=)
-/. - c.727A>G r.(?) p.(Ile243Val)
-/. - c.727A>G r.(?) p.(Ile243Val)
-?/. - c.747-16A>T r.(=) p.(=)
?/. - c.793A>G r.(?) p.(Lys265Glu)
?/. - c.825A>C r.(?) p.(Arg275Ser)
-?/. - c.885+154A>G r.(=) p.(=)
-?/. - c.885+227G>A r.(=) p.(=)
?/. - c.886-5T>A r.spl? p.?
?/. - c.886-5T>A r.spl? p.?
+/. 10i c.886-5T>A r.[886_954del,885_886inscag] p.[Val296_Gln318del,Ala295_Val296insGln]
?/. - c.937C>T r.(?) p.(Arg313Cys)
?/. - c.972G>A r.(?) p.(Met324Ile)
+/. - c.1034G>A r.(?) p.(Trp345Ter)
+/. 12 c.1042C>T r.(?) p.(Pro348Ser)
+/. 12 c.1042C>T r.(?) p.(Pro348Ser)
-/. - c.1083+4C>T r.spl? p.?
?/. - c.1091A>G r.(?) p.(Tyr364Cys)
-/. - c.1093G>C r.(?) p.(Asp365His)
-/. - c.1147+11C>T r.(=) p.(=)
-/. - c.1147+11C>T r.(=) p.(=)
-/. - c.1148-9G>C r.(=) p.(=)
-/. - c.1148-9G>C r.(=) p.(=)
?/. - c.1173A>G r.(?) p.(Ile391Met)
+/. 14 c.1187G>A r.(?) p.(Trp396*)
+?/. - c.1229dup r.(?) p.(Leu410Phefs*18)
-?/. - c.1239A>G r.(?) p.(Ser413=)
-/. - c.1242T>C r.(?) p.(Ser414=)
-/. - c.1242T>C r.(?) p.(Ser414=)
-?/. - c.1296A>G r.(?) p.(Ser432=)
-?/. - c.1296A>G r.(?) p.(Ser432=)
+/. - c.(?_1342-53)_(1580_?)dup r.0 p.0
-?/. - c.1371T>G r.(?) p.(Ser457=)
-/. - c.1371T>G r.(?) p.(Ser457=)
-/. - c.1386A>G r.(?) p.(Arg462=)
-/. - c.1386A>G r.(?) p.(Arg462=)
?/. - c.1438T>C r.(?) p.(Ser480Pro)
+?/. - c.1528C>T r.(?) p.(Arg510*)
+/. 15 c.1533_1545del r.(?) p.(Ile512Thrfs*4)
?/. - c.1573A>T r.(?) p.(Thr525Ser)
-?/. - c.1614G>A r.(?) p.(Glu538=)
?/. - c.1648G>T r.(?) p.(Gly550Cys)
-?/. - c.1686G>A r.(?) p.(Arg562=)
-?/. - c.1702G>A r.(?) p.(Val568Ile)
-?/. - c.1702G>A r.(?) p.(Val568Ile)
-?/. - c.1877+199A>C r.(=) p.(=)
-?/. - c.1878-7C>A r.(=) p.(=)
?/. - c.1919A>T r.(?) p.(Tyr640Phe)
-/. - c.1948C>T r.(?) p.(Pro650Ser)
-/. - c.1964A>G r.(?) p.(Lys655Arg)
-/. - c.1964A>G r.(?) p.(Lys655Arg)
-?/. - c.1980G>A r.(?) p.(Lys660=)
?/. - c.2048G>A r.(?) p.(Arg683His)
?/. - c.2056C>T r.(?) p.(Arg686Trp)
-/. - c.2108G>C r.(?) p.(Gly703Ala)
-?/. - c.2116C>T r.(?) p.(His706Tyr)
?/. - c.2116C>T r.(?) p.(His706Tyr)
?/. - c.2116C>T r.(?) p.(His706Tyr)
?/. - c.2116C>T r.(?) p.(His706Tyr)
-/. - c.2130G>A r.(?) p.(Gln710=)
-/. - c.2130G>A r.(?) p.(Gln710=)
?/. - c.2186C>A r.(?) p.(Ala729Glu)
?/. - c.2186C>A r.(?) p.(Ala729Glu)
+/. 20i c.2203-3C>G r.spl? p.?
+/. 20i c.2203-3C>G r.spl? p.?
-/. - c.2223G>A r.(?) p.(Leu741=)
-/. - c.2223G>A r.(?) p.(Leu741=)
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