Transcript #00018430 (NM_002972.2, SBF1 gene)

Transcript name SET binding factor 1
Gene name SBF1 (SET binding factor 1)
Chromosome 22
Transcript - NCBI ID NM_002972.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_002963.2
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

205 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-753517_*3702627del r.0? p.0?
?/. - c.55G>C r.(?) p.(Gly19Arg)
-/. - c.55+7G>A r.(=) p.(=)
-/. - c.55+9C>T r.(=) p.(=)
-?/. - c.56-19C>T r.(=) p.(=)
-?/. - c.141+10_141+12del r.(=) p.(=)
-/. - c.291C>T r.(?) p.(Arg97=)
-/. - c.296A>C r.(?) p.(Glu99Ala)
+/. - c.412C>T r.(?) p.(Arg138*)
-?/. - c.466C>T r.(?) p.(His156Tyr)
-?/. - c.498C>T r.(?) p.(Asn166=)
+/. - c.545C>T r.(?) p.(Ser182Leu)
?/. - c.549G>C r.(?) p.Gln183His
-?/. - c.549+10G>A r.(=) p.(=)
?/. - c.558C>G r.(?) p.Ile186Met
-?/. - c.603C>T r.(?) p.(Ala201=)
-?/. - c.656-6C>T r.(=) p.(=)
-?/. - c.789-18C>T r.(=) p.(=)
-?/. - c.868G>A r.(?) p.(Ala290Thr)
?/. - c.868G>A r.(?) p.(Ala290Thr)
-?/. - c.898-18G>A r.(=) p.(=)
-?/. - c.898-18G>A r.(=) p.(=)
-?/. - c.898-4G>A r.spl? p.?
?/. - c.956A>G r.(?) p.(His319Arg)
?/. - c.1031A>C r.(?) p.(Glu344Ala)
-?/. - c.1056G>A r.(?) p.(Pro352=)
-/. - c.1089+19C>T r.(=) p.(=)
-?/. - c.1164C>T r.(?) p.(Val388=)
?/. - c.1204-1G>A r.spl? p.?
+/. - c.1249A>G r.(?) p.(Met417Val)
+/. - c.1327G>A r.(?) p.(Asp443Asn)
-?/. - c.1333-4dup r.spl? p.?
?/. - c.1399G>A r.(?) p.(Val467Ile)
?/. - c.1426A>G r.(?) p.(Lys476Glu)
-?/. - c.1431+19G>A r.(=) p.(=)
-?/. - c.1432-13C>T r.(=) p.(=)
-?/. - c.1432-12G>A r.(=) p.(=)
?/. - c.1477G>A r.(?) p.(Gly493Ser)
?/. - c.1508G>C r.(?) p.(Arg503Pro)
-?/. - c.1570A>T r.(?) p.(Met524Leu)
?/. - c.1577G>T r.(?) p.(Gly526Val)
?/. - c.1583C>A r.(?) p.(Pro528His)
?/. - c.1642A>G r.(?) p.(Ile548Val)
-/. - c.1668T>C r.(?) p.(His556=)
-?/. - c.1668T>C r.(?) p.(His556=)
-?/. - c.1716C>T r.(?) p.(Tyr572=)
?/. - c.1732A>G r.(?) p.(Met578Val)
-/. - c.1749+7G>A r.(=) p.(=)
-?/. - c.1866C>T r.(?) p.(Asp622=)
-?/. - c.1899+14T>C r.(=) p.(=)
-?/. - c.1899+16C>T r.(=) p.(=)
-?/. - c.1947T>A r.(?) p.(Pro649=)
?/. - c.1966C>T r.(?) p.(Arg656Trp)
-?/. - c.1968+15G>A r.(=) p.(=)
-/. - c.1968+15G>A r.(=) p.(=)
-/. - c.1980G>A r.(?) p.(Pro660=)
-?/. - c.2034G>A r.(?) p.(Thr678=)
-?/. - c.2034G>A r.(?) p.(Thr678=)
-?/. - c.2079C>T r.(?) p.(His693=)
-/. - c.2079C>T r.(?) p.(His693=)
?/. - c.2084G>A r.(?) p.(Arg695Gln)
-/. - c.2106G>A r.(?) p.(Thr702=)
-?/. - c.2121C>G r.(?) p.(Pro707=)
-/. - c.2128-17G>A r.(=) p.(=)
?/. - c.2140G>T r.(?) p.(Ala714Ser)
-/. - c.2175C>T r.(?) p.(Asp725=)
-?/. - c.2463C>T r.(?) p.(Asp821=)
?/. - c.2563G>T r.(?) p.(Val855Leu)
-/. - c.2569+4C>T r.spl? p.?
-?/. - c.2569+4C>T r.spl? p.?
-?/. - c.2569+16C>T r.(=) p.(=)
-?/. - c.2570-3C>T r.spl? p.?
?/. - c.2570-1G>T r.spl? p.?
?/. - c.2605G>A r.(?) p.(Val869Met)
-?/. - c.2688G>A r.(?) p.(Val896=)
-?/. - c.2697C>A r.(?) p.(Gly899=)
-/. - c.2712G>C r.(?) p.(Leu904=)
-?/. - c.2737G>A r.(?) p.(Ala913Thr)
?/. - c.2737G>A r.(?) p.(Ala913Thr)
?/. - c.2774C>G r.(?) p.(Ala925Gly)
-?/. - c.2784C>T r.(?) p.(Ala928=)
?/. 23 c.2885C>T r.(?) p.(Thr962Ile)
-?/. - c.2955C>T r.(?) p.(Ser985=)
-?/. - c.2967+9C>A r.(=) p.(=)
-/. - c.3006C>T r.(?) p.(Asp1002=)
-?/. - c.3012C>T r.(?) p.(=)
?/. - c.3044G>A r.(?) p.(Arg1015Gln)
?/. - c.3044G>A r.(?) p.(Arg1015Gln)
-?/. - c.3147-8G>C r.(=) p.(=)
?/. - c.3191G>A r.(?) p.(Gly1064Glu)
?/. - c.3221A>C r.(?) p.(Asn1074Thr)
?/. - c.3250C>A r.(?) p.(Pro1084Thr)
-?/. - c.3250C>A r.(?) p.(Pro1084Thr)
?/. - c.3251C>T r.(?) p.(Pro1084Leu)
-?/. - c.3294G>A r.(?) p.(Glu1098=)
-?/. - c.3294G>A r.(?) p.(Glu1098=)
?/. - c.3302C>A r.(?) p.(Pro1101His)
?/. - c.3308C>T r.(?) p.(Thr1103Met)
-/. - c.3339C>T r.(?) p.(Ser1113=)
?/. - c.3340G>A r.(?) p.(Asp1114Asn)
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