ClinVar Miner

Submissions for variant NM_000038.6(APC):c.-19G>C

dbSNP: rs1064793813
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000479397 SCV000569984 uncertain significance not provided 2016-04-13 criteria provided, single submitter clinical testing This variant is denoted APC c.-19G>C, and describes a nucleotide substitution, in the 5' untranslated region (UTR), 19 base pairs upstream of the APC ATG translational start site, which is located in exon 2. This variant does not appear to affect the start codon or the Kozak translational consensus sequence and has not, to our knowledge, been published in the literature as pathogenic or benign. Multiple splicing models predict that this variant may damage or destroy a natural splice donor site for intron 1; however, it is unknown whether this change will affect the promoter and/or protein translation. APC c.-19G>C occurs at a position that is conserved and is not covered in the NHLBI Exome Sequencing Project. At this time, we consider APC c.-19G>C to be a variant of uncertain significance.

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