ClinVar Miner

Submissions for variant NM_004260.4(RECQL4):c.897del (p.Glu301fs)

dbSNP: rs2130720341
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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 RCV001381590 SCV001580030 pathogenic Baller-Gerold syndrome 2023-08-28 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 1069662). For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals affected with RECQL4-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Glu301Asnfs*58) 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).

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