Transcript #00018432 (NM_030962.3, SBF2 gene)

Transcript name SET binding factor 2
Gene name SBF2 (SET binding factor 2)
Chromosome 11
Transcript - NCBI ID NM_030962.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_112224.1
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.56-64G>A r.(=) p.(=)
+/. - c.134T>A r.(?) p.(Ile45Asn)
+/. - c.141+1G>A r.spl p.(?)
?/. - c.141+128A>G r.(=) p.(=)
-/. - c.142-14dup r.(=) p.(=)
-?/. - c.142-14dup r.(=) p.(=)
?/. - c.161G>A r.(?) p.(Trp54Ter)
+/. - c.178_179del r.(?) p.(Arg60Glufs*14)
?/. - c.364G>A r.(?) p.(Val122Met)
?/. - c.422A>G r.(?) p.(Tyr141Cys)
-/. - c.513+17G>C r.(=) p.(=)
-?/. - c.513+18A>T r.(=) p.(=)
-/. - c.514-53A>T r.(=) p.(=)
-/. - c.620-75T>C r.(=) p.(=)
+?/. - c.620G>T r.(?) p.(Gly207Val)
-/. - c.753-16T>A r.(=) p.(=)
-/. - c.753-16T>A r.(=) p.(=)
-/. - c.753-16T>A r.(=) p.(=)
?/. - c.777G>A r.(?) p.(Pro259=)
?/. - c.777G>A r.(?) p.(Pro259=)
?/. - c.862-7C>G r.spl? p.(?)
-/. - c.909C>T r.(?) p.(Pro303=)
-/. - c.909C>T r.(=) p.(=)
?/. - c.1124A>G r.(?) p.(Gln375Arg)
?/. - c.1166A>G r.(?) p.(Lys389Arg)
-/. - c.1167+74C>T r.(=) p.(=)
-/. - c.1167+75G>T r.(=) p.(=)
-/. - c.1167+165_1167+166dup r.(=) p.(=)
-/. - c.1173A>G r.(?) p.(Ala391=)
?/. - c.1291G>A r.(?) p.(Asp431Asn)
+/. - c.1291G>C r.(?) p.(Asp431His)
-/. - c.1395+80T>G r.(=) p.(=)
+?/. - c.(1395+1_1396-1)_(3652+1_3653-1)del r.? p.?
+/. - c.1459C>T r.(?) p.(Arg487Ter)
+/. 14 c.1459C>T r.(?) p.(Arg487*)
-?/. - c.1509A>G r.(?) p.(Glu503=)
+/. 14 c.1537C>T r.(?) p.(Gln513*)
+/. 14i c.1601-2A>G r.1601_1617del p.Val534Glyfs*23
-/. - c.1861-62C>G r.(=) p.(=)
-?/. - c.1893C>T r.(?) p.(Ala631=)
-?/. - c.1929+7T>C r.(=) p.(=)
?/. - c.1967G>C r.(?) p.(Cys656Ser)
-/. - c.2035G>A r.(?) p.(Glu679Lys)
-/. - c.2035G>A r.(?) p.(Glu679Lys)
?/. - c.2045G>A r.(?) p.(Arg682His)
?/. - c.2101-66del r.(=) p.(=)
?/. - c.2101G>A r.(?) p.(Asp701Asn)
?/. - c.2164C>T r.(?) p.(Arg722Cys)
-?/. - c.2197C>G r.(?) p.(Gln733Glu)
?/. - c.2197C>G r.(?) p.(Gln733Glu)
+?/. - c.2215G>A r.(?) p.(Glu739Lys)
-?/. - c.2319G>A r.(?) p.(Ala773=)
-?/. - c.2323G>A r.(?) p.(Gly775Ser)
-?/. - c.2323G>A r.(?) p.(Gly775Ser)
-?/. - c.2323G>A r.(?) p.(Gly775Ser)
-/. - c.2364-94C>A r.(=) p.(=)
?/. - c.2424T>A r.(?) p.(Asn808Lys)
+?/. - c.2536+1G>A r.spl p.?
-/. - c.2537-209A>C r.(=) p.(=)
+/. - c.2578C>T r.(?) p.(Arg860*)
+/. - c.2578C>T r.(?) p.(Arg860*)
+/. - c.2597del r.(?) p.(Pro866Argfs*70)
+/. - c.2597del r.(?) p.(Pro866Argfs*70)
-/. - c.2611-19_2611-16del r.(=) p.(=)
-?/. - c.2611-19_2611-16dup r.(=) p.(=)
+/. - c.2678T>C r.(?) p.(Leu893Pro)
+/. - c.2678T>C r.(?) p.(Leu893Pro)
+/. - c.2678T>C r.(?) p.(Leu893Pro)
-/. - c.2807-8A>G r.(=) p.(=)
-/. - c.2850C>T r.(?) p.(Ile950=)
+/. - c.2875C>T r.(?) p.(Gln959Ter)
+/. 23 c.2875C>T r.(?) p.(Gln959*)
-?/. - c.3036C>T r.(?) p.(Thr1012=)
-/. - c.3111-6T>C r.(=) p.(=)
?/. - c.3256+47T>C r.(=) p.(=)
?/. - c.3290C>A r.(?) p.(Thr1097Asn)
?/. - c.3290C>A r.(?) p.(Thr1097Asn)
-?/. - c.3292C>G r.(?) p.(Leu1098Val)
-/. - c.3292C>G r.(?) p.(Leu1098Val)
?/. - c.3376A>T r.(?) p.(Ile1126Leu)
-/. - c.3455+36C>T r.(=) p.(=)
-?/. - c.3456-22_3456-18del r.(=) p.(=)
-?/. - c.3572G>A r.(?) p.(Gly1191Asp)
+/. - c.3586C>T r.(?) p.(Arg1196Ter)
+/. 27 c.3586C>T r.(?) p.(Arg1196*)
-/. - c.3646C>G r.(?) p.(Gln1216Glu)
-/. - c.3646C>G r.(?) p.(Gln1216Glu)
-?/. - c.3652+15A>G r.(=) p.(=)
-?/. - c.3730G>T r.(?) p.(Val1244Phe)
-?/. - c.3793+19T>G r.(=) p.(=)
-/. - c.3794-20C>T r.(=) p.(=)
-?/. - c.3819C>T r.(?) p.(Ser1273=)
?/. - c.3866G>A r.(?) p.(Arg1289Gln)
-?/. - c.3877A>G r.(?) p.(Lys1293Glu)
+/. 29 c.3946del r.(?) p.(Leu1316Phefs*10)
?/. - c.4065G>T r.(?) p.(Lys1355Asn)
-/. - c.4156-46C>T r.(=) p.(=)
-?/. - c.4209T>C r.(?) p.(Gly1403=)
+/. 32 c.4299G>C r.(?) p.(Arg1433Ser)
+/. - c.4443+1G>C r.spl? p.?
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