Candidate colorectal cancer predisposing genes with Sanger validated truncating variants in familial CRC cases.
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资源简介：
Gene, transcript and chromosomal positions taken from Ensembl build 37 (http://www.ensembl.org).afs = frameshift insertion and deletion variant, sp = splice site variant.bCounts include both exome data controls and Sanger sequenced controls.
创建时间：
2015-12-02
