ClinVar Miner

Submissions for variant NM_005214.5(CTLA4):c.494G>A (p.Trp165Ter)

dbSNP: rs2469720798
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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 RCV003079037 SCV003460736 pathogenic Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency 2022-03-28 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Trp165*) in the CTLA4 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in CTLA4 are known to be pathogenic (PMID: 25213377, 25329329). This variant is not present in population databases (gnomAD no frequency). This premature translational stop signal has been observed in individual(s) with CTLA4 haploinsufficiency (PMID: 28960754, 30048690). For these reasons, this variant has been classified as Pathogenic.

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