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History Report on CCDS ID 47925 Re-query CCDS DB by CCDS ID:47925

InterpretationDateSourceCommentData
CCDS: Made public 09/02/2009 NCBI CCDS Release: 6
CCDS: Public note 08/09/2010 NCBI The coding region has been updated to shorten the N-terminus to one that is supported by the reference genome allele (GRCh37 assembly). The previous representation used a polymorphic start codon that exists as ACG in the reference genome allele versus ATG in the alternate allele (also known as the T allele). This corresponds to the reference SNP rs2294008. Some individuals contain the reference genome allele, while others contain the T allele. Data in PMIDs 18488030, 19554573, 19582881 and 19648920 indicate that the T allele may be a risk allele for gastric and bladder cancers. It is also associated with decreased promoter activity (PMIDs 18488030 and 19648920). The current update results in a protein that is 9 aa shorter at the N-terminus. CCDS version: 47925.1
CCDS: Partial match 03/30/2011 NCBI CCDS Release: 8
CCDS: Partial match 08/11/2011 NCBI CCDS Release: 9
CCDS: Reinstated 09/19/2012 NCBI CCDS Release: 11
CCDS: Updated 09/19/2012 NCBI CCDS Release: 11
CCDS: Retained 03/21/2013 NCBI CCDS Release: 12
CCDS: Retained 08/30/2013 NCBI CCDS Release: 14
CCDS: Retained 11/21/2013 NCBI CCDS Release: 15
CCDS: Retained 06/20/2014 NCBI CCDS Release: 17
CCDS: Retained 04/03/2015 NCBI CCDS Release: 18
CCDS: Retained 08/11/2016 NCBI CCDS Release: 20
CCDS: Review status 10/03/2016 NCBI by RefSeq, Havana and CCDS collaboration
CCDS: Retained 05/16/2018 NCBI CCDS Release: 22
CCDS: Retained 08/10/2022 NCBI CCDS Release: 24


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