ClinVar

Description

The c.258+2T>C intronic pathogenic mutation results from a T to C substitution two nucleotides after coding exon 2 in the SBDS gene. This mutation has been described in multiple individuals with Shwachman-Diamond syndrome; it has been reported in homozygous individuals and is also known to occur as part of a complex allele: c.[183_184delTAinsCT;258+2T>C] (Boocock GR et al. Nat. Genet., 2003 Jan;33:97-101). In a study of seven individuals with c.258+2T>C in trans with a second mutation, each had a history of pancreatic insufficiency, four had skeletal abnormalities, and two had hematological malignancies (Kawakami T et al. Tohoku J. Exp. Med., 2005 Jul;206:253-9). RT-PCR identified a deletion of 8 base pairs at the end of exon 2 in some affected individuals; gene sequencing revealed the c.258+2T>C alteration in these individuals, which would be consistent with the use of an upstream cryptic splice donor predicted to result in an 8 base pair deletion leading to a frameshift and premature protein truncation (p.C84Yfs*4; Boocock GR et al. Nat. Genet., 2003 Jan;33:97-101). In addition to the clinical data presented in the literature, alterations that disrupt the canonical splice site are expected to cause aberrant splicing, resulting in an abnormal protein or a transcript that is subject to nonsense-mediated mRNA decay. As such, this alteration is classified as pathogenic.