ClinVar Miner

Submissions for variant NM_004260.4(RECQL4):c.805del (p.Trp269fs)

dbSNP: rs1060501370
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000465867 SCV000545924 pathogenic Baller-Gerold syndrome 2024-05-22 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Trp269Glyfs*24) in the RECQL4 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in RECQL4 are known to be pathogenic (PMID: 12734318, 12952869). This variant is present in population databases (no rsID available, gnomAD 0.0009%). This variant has not been reported in the literature in individuals affected with RECQL4-related conditions. ClinVar contains an entry for this variant (Variation ID: 406956). For these reasons, this variant has been classified as Pathogenic.

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