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HomeAll Cancer Mutant ClonesMYCN Mutants

Description of the mutations of MYCN (NM_005378) Mutants

Keys for Mutation Description

A.A. substitution
NT deletion
NT insertion
R280G: Arg at aa-position 280 mutated to Gly
R342X: R at aa-position 342 mutated to a stop codon and caused truncation of the protein
N268_D2: The deletion starts at nt#268. Two bases (including nt268) are deleted
N478-I6: The insertion starts after nt#478. Six bases are inserted


SKUMutation DescriptionAffected Codon#Affected NT#DescriptionEffect
RC402779 E73X73217G>TFeingold syndrome
RC402780 W77X77231G>AFeingold syndrome
RC402781 G151X151451G>TFeingold syndrome
RC402782 S221X221662C>AFeingold syndrome
RC402783 R322X322964C>TFeingold syndrome
RC402784 R373X3731117C>TFeingold syndrome
RC402785 R382H3821145G>AFeingold syndrome
RC402786 R393H3931178G>AFeingold syndrome
RC402787 R393S3931177C>AFeingold syndrome
RC402788 R394H3941181G>AFeingold syndrome
RC402789 P409L4091226C>TFeingold syndrome


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