ClinVar Miner

Submissions for variant NM_006019.4(TCIRG1):c.530_537del (p.His177fs)

dbSNP: rs1295614525
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001915986 SCV002181155 pathogenic not provided 2023-09-27 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 1406783). This variant has not been reported in the literature in individuals affected with TCIRG1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.His177Profs*47) in the TCIRG1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in TCIRG1 are known to be pathogenic (PMID: 10888887, 10942435, 11532986, 19448635).
Baylor Genetics RCV004571586 SCV005052944 likely pathogenic Autosomal recessive osteopetrosis 1 2024-03-04 criteria provided, single submitter clinical testing

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