Transcript #00000127 (NM_005378.4, MYCN gene)

Transcript name v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian)
Gene name MYCN (v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian))
Chromosome 2
Transcript - NCBI ID NM_005378.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005369.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-05-11 13:12:11 +02:00 (CEST)
Date last edited N/A


Variants

63 entries on 1 page. Showing entries 1 - 63.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-214G>T r.(?) p.(=)
-?/. - c.-214G>T r.(?) p.(=)
?/. - c.-195G>C r.(?) p.(=)
?/. - c.-183G>C r.(?) p.(=)
-?/. - c.-179C>G r.(?) p.(=)
-?/. - c.-177C>T r.(?) p.(=)
-?/. - c.-170A>C r.(?) p.(=)
?/. - c.-129A>G r.(?) p.(=)
?/. - c.-118+290del r.(=) p.(=)
?/. - c.-59del r.(?) p.(=)
-?/. - c.-24A>T r.(?) p.(=)
-?/. - c.18G>A r.(?) p.(Thr6=)
-?/. - c.90G>C r.(?) p.(Pro30=)
?/. - c.109T>A r.(?) p.(Phe37Ile)
-?/. - c.111C>A r.(?) p.(Phe37Leu)
+/. - c.134dup r.(?) p.(Glu47GlyfsTer8)
+/. - c.204_205del r.(?) p.(Glu69AlafsTer15)
+/. - c.204_205del r.(?) p.(Glu69AlafsTer15)
-?/. - c.207G>A r.(?) p.(Glu69=)
-?/. - c.227G>T r.(?) p.(Ser76Ile)
+?/. - c.266dup r.(?) p.(Ser90Glnfs*176)
-?/. - c.279G>C r.(?) p.(Glu93Asp)
?/. - c.279G>C r.(?) p.(Glu93Asp)
-?/. - c.311G>A r.(?) p.(Gly104Asp)
+/. - c.394G>T r.(?) p.(Glu132Ter)
-?/. - c.430G>A r.(?) p.(Gly144Ser)
?/. - c.451G>C r.(?) p.(Gly151Arg)
-?/. - c.470C>T r.(?) p.(Pro157Leu)
-?/. - c.499G>A r.(?) p.(Gly167Arg)
+/. - c.499G>T r.(?) p.(Gly167*)
-?/. - c.500G>A r.(?) p.(Gly167Glu)
-?/. - c.501A>G r.(?) p.(Gly167=)
-?/. - c.509G>C r.(?) p.(Arg170Pro)
-?/. - c.517G>A r.(?) p.(Ala173Thr)
?/. - c.535C>G r.(?) p.(Leu179Val)
-?/. - c.658G>C r.(?) p.(Ala220Pro)
-?/. - c.658G>T r.(?) p.(Ala220Ser)
-?/. - c.713G>C r.(?) p.(Arg238Pro)
-?/. - c.753C>T r.(?) p.(Ala251=)
?/. - c.799G>T r.(?) p.(Asp267Tyr)
?/. - c.807_809del r.(?) p.(Glu271del)
?/. - c.816T>G r.(?) p.(Asp272Glu)
?/. - c.920C>T r.(?) p.(Ala307Val)
+?/. - c.940C>T r.(?) p.(Gln314*)
+/. - c.964C>T r.(?) p.(Arg322*)
-?/. - c.1062G>A r.(?) p.(Ala354=)
?/. - c.1093C>G r.(?) p.(Pro365Ala)
?/. - c.1145G>A r.(?) p.(Arg382His)
+?/. - c.1145G>C r.(?) p.(Arg382Pro)
./. - c.1148G>A r.(?) p.(Arg383His)
+?/. - c.1172G>T r.(?) p.(Arg391Leu)
+/. - c.1177C>T r.(?) p.(Arg393Cys)
+/. - c.1178G>A r.(?) p.(Arg393His)
+/. - c.1180C>T r.(?) p.(Arg394Cys)
+/. - c.1181G>A r.(?) p.(Arg394His)
+?/. - c.1192C>T r.(?) p.(Arg398Trp)
+?/. - c.1205T>C r.(?) p.(Leu402Pro)
-?/. - c.1208C>T r.(?) p.(Thr403Met)
?/. - c.1271A>G r.(?) p.(Lys424Arg)
+/. - c.1282G>T r.(?) p.(Glu428Ter)
+?/. - c.1319T>C r.(?) p.(Leu440Pro)
+?/. - c.1325T>C r.(?) p.(Leu442Pro)
-?/. - c.1367A>G r.(?) p.(Lys456Arg)
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