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HomeAll Cancer Mutant ClonesROR2 Mutants

Description of the mutations of ROR2 (NM_004560) 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
RC402742 R119X119355C>TRobinow syndrome, autosomal recessive
RC402743 C182Y182545G>ARobinow syndrome, autosomal recessive
RC402744 R184C184550C>TRobinow syndrome, autosomal recessive
RC402745 R189W189565C>TRobinow syndrome, autosomal recessive
RC402746 Y192D192574T>GRobinow syndrome, autosomal recessive
RC402747 R205X205613C>TRobinow syndrome, autosomal recessive
RC402748 R244W244730C>TRobinow syndrome, autosomal recessive
RC402749 R366W3661096C>TRobinow syndrome, autosomal recessive
RC402750 R397X3971189C>TRobinow syndrome, autosomal recessive
RC402751 Q502X5021504C>TRobinow syndrome, autosomal recessive
RC402752 N620K6201860T>ARobinow syndrome, autosomal recessive
RC402753 W720X7202160G>ARobinow syndrome, autosomal recessive
RC402754 W749X7492247G>ABrachydactyly, type B
RC402755 W749X7492246G>ABrachydactyly, type B
RC402756 Y755X7552265C>ABrachydactyly, type B
RC402757 Q760X7602278C>TBrachydactyly, type B


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