Transcript #00018034 (NM_022370.3, ROBO3 gene)

Transcript name roundabout, axon guidance receptor, homolog 3 (Drosophila)
Gene name ROBO3 (roundabout, axon guidance receptor, homolog 3 (Drosophila))
Chromosome 11
Transcript - NCBI ID NM_022370.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_071765.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

76 entries on 1 page. Showing entries 1 - 76.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.161-10del r.(=) p.(=)
+?/. - c.274C>T r.(?) p.(Arg92*)
?/. - c.302G>A r.(?) p.(Gly101Glu)
?/. - c.384C>A r.(?) p.(Ile128=)
-?/. - c.488-6G>C r.(=) p.(=)
-?/. - c.488-2_488-1del r.spl? p.?
-?/. - c.488-2_488del r.spl? p.?
-?/. - c.488T>C r.(?) p.(Val163Ala)
-?/. - c.491T>C r.(?) p.(Leu164Pro)
+/. - c.571dup r.(?) p.(Arg191ProfsTer61)
+?/. - c.571dup r.(?) p.(Arg191ProfsTer61)
-/. - c.726G>C r.(?) p.(Ala242=)
?/. - c.769C>T r.(?) p.(Arg257Cys)
?/. - c.850G>A r.(?) p.(Asp284Asn)
?/. - c.850G>A r.(?) p.(Asp284Asn)
?/. - c.874C>T r.(?) p.(Arg292Cys)
-?/. - c.968C>T r.(?) p.(Thr323Met)
?/. - c.968C>T r.(?) p.(Thr323Met)
-?/. - c.1267G>A r.(?) p.(Val423Met)
-?/. - c.1267G>A r.(?) p.(Val423Met)
+?/. - c.1425_1438del r.(?) p.(Gly476GlnfsTer15)
+/. - c.1447C>T r.(?) p.(Arg483Ter)
+?/. - c.1469G>A r.(?) p.(Trp490*)
-/. - c.1615C>T r.(?) p.(Arg539Trp)
-?/. - c.1616G>A r.(?) p.(Arg539Gln)
?/. - c.1667C>T r.(?) p.(Pro556Leu)
?/. - c.1805G>T r.(?) p.(Trp602Leu)
?/. - c.1838C>T r.(?) p.(Thr613Ile)
-?/. - c.1838C>T r.(?) p.(Thr613Ile)
-?/. - c.1852G>A r.(?) p.(Gly618Ser)
-?/. - c.1852G>A r.(?) p.(Gly618Ser)
?/. - c.1868C>A r.(?) p.(Thr623Asn)
?/. - c.1951+3A>G r.spl? p.?
-?/. - c.1951+10G>A r.(=) p.(=)
+/. - c.2107C>T r.(?) p.(Arg703Trp)
-?/. - c.2169C>A r.(?) p.(Ser723=)
?/. - c.2308G>T r.(?) p.(Gly770Cys)
?/. - c.2308G>T r.(?) p.(Gly770Cys)
-?/. - c.2310C>T r.(?) p.(Gly770=)
?/. - c.2413G>T r.(?) p.(Glu805Ter)
?/. - c.2437A>C r.(?) p.(Asn813His)
?/. - c.2618G>T r.(?) p.(Gly873Val)
-?/. - c.2621T>A r.(?) p.(Leu874Gln)
-?/. - c.2632G>A r.(?) p.(Ala878Thr)
?/. - c.2695G>T r.(?) p.(Ala899Ser)
?/. - c.2763G>C r.(?) p.(Glu921Asp)
?/. - c.2771A>G r.(?) p.(His924Arg)
-?/. - c.2779+10C>T r.(=) p.(=)
-?/. - c.2781C>G r.(?) p.(=)
+?/. - c.2901_2902del r.(?) p.(His968ProfsTer17)
?/. - c.2957A>C r.(?) p.(Asn986Thr)
-/. - c.2991G>A r.(?) p.(Ala997=)
?/. - c.2993G>T r.(?) p.(Gly998Val)
?/. - c.3056A>G r.(?) p.(Tyr1019Cys)
-?/. - c.3593G>A r.(?) p.(Arg1198His)
-?/. - c.3593G>A r.(?) p.(Arg1198His)
?/. - c.3599C>T r.(?) p.(Ala1200Val)
-?/. - c.3641A>C r.(?) p.(His1214Pro)
-?/. - c.3652A>G r.(?) p.(Ser1218Gly)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
-?/. - c.3796+6G>A r.(=) p.(=)
?/. - c.3848T>G r.(?) p.(Leu1283Arg)
+?/. - c.3937C>T r.(?) p.(Gln1313*)
-?/. - c.3958+5G>A r.spl? p.?
-?/. - c.4001G>C r.(?) p.(Arg1334Pro)
?/. - c.4025C>G r.(?) p.(Ser1342Cys)
-?/. - c.4075C>A r.(?) p.(Arg1359=)
-/. - c.4100_4105del r.(?) p.(Arg1367_Ser1368del)
-?/. - c.4116C>A r.(?) p.(Ser1372Arg)
?/. - c.4148A>G r.(?) p.(Glu1383Gly)
-/. - c.*3788C>T r.(=) p.(=)
-?/. - c.*3788C>T r.(=) p.(=)
-?/. - c.*3901A>G r.(=) p.(=)
-?/. - c.*3970T>A r.(=) p.(=)
?/. - c.*3973C>T r.(=) p.(=)
-?/. - c.*3973C>T r.(=) p.(=)
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