ClinVar Miner

Submissions for variant NM_006019.4(TCIRG1):c.1459del (p.Trp487fs)

dbSNP: rs2134455711
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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 RCV001946970 SCV002238736 pathogenic not provided 2020-10-28 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals with TCIRG1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Trp487Glyfs*41) 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).
Fulgent Genetics, Fulgent Genetics RCV002507703 SCV002813992 likely pathogenic Autosomal recessive osteopetrosis 1 2022-05-27 criteria provided, single submitter clinical testing

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