ClinVar Miner

Submissions for variant NM_002615.7(SERPINF1):c.77dup (p.Glu27fs)

dbSNP: rs1272920425
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics RCV001839466 SCV002099532 pathogenic Osteogenesis imperfecta type 6 2021-09-27 criteria provided, single submitter clinical testing A heterozygous single base-pair duplication in exon 2 of the SERPINF1 gene that results in a frameshift and premature truncation of protein 38 amino acids downstream to codon 27 was detected. The observed variant c.77dup (p.Glu27GlyfsTer38) has not been reported in the 1000 genomes and gnomAD database. The variant has previously been reported in patients affected with osteogenesis imperfecta (Li et al. 2020). The in silico prediction of the variant is damaging by MutationTaster2. The reference codon is conserved across primates. In summary, the variant meets our criteria to be classified as a pathogenic variant.

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