SLOT THR777 THINGS TO KNOW BEFORE YOU BUY

ClinVar has an entry for this variant (Variation ID: 574387). Variants that disrupt the consensus splice website are a relatively popular reason for aberrant splicing (PMID: 17576681, 9536098). Algorithms produced to predict the outcome of sequence adjustments on RNA splicing recommend that this variant may well build or improve a splice web-site.