Splicing analysis in CA8-204 reveals cryptic splice sites in rs6471859 created with “G” allele.

Results of splicing analyses from HSF3.1 (http://www.umd.be/HSF3/HSF.shtml) for the CA8-204 sequence (NCBI accession: NM_001321837.1, NG_023193.2, refSNP or clinical variation: rs6471859) with the “G” allele at 1,416 bp (SNP location within CA8-204 transcript) and when it is replaced with “C” allele at position 1,416 bp (SNP variation) 0–100, < -10: splice site disrupted; >30: splice site formed. Consensus value is calculated based on the possibility of production of a cryptic splice site within the sequences, ranging from 0–100, <10- splice site disrupted; >30- Splice site formed. The sequence containing the SNP has been highlighted in bold and underlined.