Transcript #00025295 (NM_001190274.1, FBXO11 gene)

Transcript name transcript variant 4
Gene name FBXO11 (F-box protein 11)
Chromosome 2
Transcript - NCBI ID NM_001190274.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001177203.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

603 entries on 7 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.109C>T r.(?) p.(Gln37Ter)
-?/. - c.120_134del r.(?) p.(Gln42_Pro46del)
-?/. - c.146C>A r.(?) p.(Pro49Gln)
-?/. - c.149A>C r.(?) p.(Gln50Pro)
-?/. - c.167_169del r.(?) p.(Gln56del)
-?/. - c.167_169dup r.(?) p.(Gln56dup)
-?/. - c.167_169dup r.(?) p.(Gln56dup)
+/. - c.233-19_1398+22del r.? p.?
+?/. - c.319_320del r.(?) p.(Leu107Alafs*45)
+?/. - c.404A>G r.(?) p.(Lys135Arg)
+?/. - c.414A>T r.(?) p.(Arg138Ser)
+/. - c.440C>G r.(?) p.(Ser147Ter)
?/. - c.442G>A r.(?) p.(Ala148Thr)
+/. - c.442+1dup r.spl? p.?
./. - c.442+1dup r.spl? p.?
+?/. - c.467A>G r.(?) p.(Gln156Arg)
+?/. - c.506_507del r.(?) p.(Ser169Leufs*9)
./. - c.552del r.(?) p.(Lys184Asnfs*27)
?/. - c.596T>C r.(?) p.(Leu199Ser)
-?/. - c.599A>T r.(?) p.(Tyr200Phe)
./. - c.606A>C r.(?) p.(Glu202Asp)
./. - c.668del r.(?) p.(Pro223Glnfs*23)
?/. - c.947T>G r.(?) p.(Val316Gly)
+?/. - c.1042-1G>C r.spl p.?
+?/. - c.1046dup r.(?) p.(Asn349LysfsTer3)
+?/. - c.1260+1G>C r.spl p.?
./. - c.1517A>G r.(?) p.(Tyr506Cys)
-?/. - c.1549G>C r.(?) p.(Glu517Gln)
+?/. - c.1612A>G r.(?) p.(Ile538Val)
+?/. - c.1648G>C r.(?) p.(Gly550Arg)
?/. - c.1660T>G r.(?) p.(Phe554Val)
./. - c.1660T>G r.(?) p.(Phe554Val)
+?/. - c.1706A>G r.(?) p.(Asn569Ser)
./. - c.1781A>G r.(?) p.(His594Arg)
./. - c.1798-1G>A r.spl? p.?
+?/. - c.1825_1829del r.(?) p.(Glu609*)
./. - c.1830T>G r.(?) p.(Asn610Lys)
+?/. - c.1868C>G r.(?) p.(Thr623Arg)
./. - c.1967A>G r.(?) p.(Asn656Ser)
./. - c.2060G>A r.(?) p.(Gly687Asp)
./. - c.2074T>A r.(?) p.(Tyr692Asn)
./. - c.2075A>T r.(?) p.(Tyr692Phe)
+?/. - c.2084-6_2085dup r.spl p.?
+?/. - c.2084-1G>A r.spl p.?
./. - c.2145G>C r.(?) p.(Lys715Asn)
./. - c.2145G>C r.(?) p.(Lys715Asn)
+?/. - c.2171_2173del r.(?) p.(Arg724del)
?/. - c.2171_2173del r.(?) p.(Arg724del)
+?/. - c.2211_2217del r.(?) p.(Ile737Metfs*30)
./. - c.2395_2397del r.(?) p.(Asn799del)
?/. - c.2398C>T r.(?) p.(Arg800Trp)
-?/. - c.2446+8G>A r.(=) p.(=)
-?/. - c.2491A>G r.(?) p.(Ser831Gly)
+?/. - c.2518T>C r.(?) p.(Ser840Pro)
./. - c.2520_2521del r.(?) p.(Ser841Leufs*8)
./. - c.2568_2572del r.(?) p.(Asn857Hisfs*12)
./. - c.2570_2572del r.(?) p.(Asn857del)
./. - c.2592_2593del r.(?) p.(Ile864Metfs*6)
./. - c.2592_2593del r.(?) p.(Ile864Metfs*6)
+?/. - c.2675C>A r.(?) p.(Ala892Asp)
./. - c.2685_2686del r.(?) p.(Ser896*)
+?/. - c.2700_2703dup r.(?) p.(Ala902Ilefs*4)
+?/. - c.2709dup r.(?) p.(Glu904*)
+?/. - c.2714C>G r.(?) p.(Pro905Arg)
+?/. - c.2729A>G r.(?) p.(Asp910Gly)
+/. - c.2738_2739del r.(?) p.(Tyr913*)
./. - c.2738_2739del r.(?) p.(Tyr913*)
+?/. 23 c.2738_2739del r.(?) p.(Tyr913*)
./. - c.2738_2739del r.(?) p.(Tyr913*)
+?/. - c.2738_2739del r.(?) p.(Tyr913*)
./. - c.2748_2749del r.(?) p.(Pro917Thrfs*5)
-/. - c.*1173A>T r.(=) p.(=)
?/. - c.*1181_*1182dup r.(=) p.(=)
-?/. - c.*1272_*1275dup r.(=) p.(=)
-?/. - c.*1272_*1275dup r.(=) p.(=)
-?/. - c.*1272_*1275dup r.(=) p.(=)
-?/. - c.*1272_*1275dup r.(=) p.(=)
?/. - c.*1319_*1320insTCCTT r.(=) p.(=)
?/. - c.*1337T>G r.(=) p.(=)
-?/. - c.*1347_*1348del r.(=) p.(=)
?/. - c.*1347_*1365del r.(=) p.(=)
-?/. - c.*1349A>T r.(=) p.(=)
?/. - c.*1349A>T r.(=) p.(=)
-/. - c.*1364_*1366del r.(=) p.(=)
-/. - c.*1365_*1366del r.(=) p.(=)
-/. - c.*1366del r.(?) p.(=)
-/. - c.*1366del r.(?) p.(=)
-/. - c.*1366del r.(?) p.(=)
-/. - c.*1366dup r.(?) p.(=)
-?/. - c.*1366dup r.(?) p.(=)
-/. - c.*1366dup r.(?) p.(=)
-/. - c.*1436_*1449dup r.(=) p.(=)
-?/. - c.*1441_*1465del r.(=) p.(=)
-?/. - c.*1452T>C r.(=) p.(=)
-?/. - c.*1460_*1464dup r.(=) p.(=)
-?/. - c.*1462_*1465del r.(=) p.(=)
-?/. - c.*1462_*1465del r.(=) p.(=)
-?/. - c.*1462_*1465del r.(=) p.(=)
-/. - c.*1462_*1465del r.(=) p.(=)
-/. - c.*1462_*1465dup r.(=) p.(=)
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