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ClinVar has an entry for this variant (Variation ID: 574387). Variants that disrupt the consensus splice site are a relatively popular cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms formulated to forecast the result of sequence changes on RNA splicing counsel that this variant might create or strengthen a splice site. In summary,
Prilika da se razgovara i da se razmene ideje: učesnici diskusije u KumanovuFoto: Pandeli Pani/DW „Ratovi iz 1990-ih i dalje imaju uticaj na društva na Zapadnom Balkanu. Ovde je važno da se konstruktivnim idejama suprotstavimo predrasudama i tenzijama, i da damo glas mladoj generaciji“, objašnjava inicijatorka projekta, urednica DW programa