ClinVar Miner

Submissions for variant NM_000538.4(RFXAP):c.524_527del (p.Lys175fs)

dbSNP: rs2138213000
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago RCV002053870 SCV002320669 pathogenic MHC class II deficiency 2022-01-10 criteria provided, single submitter clinical testing RFXAP NM_000538.3 exon 1 p.Lys175Srgfs*8 (c.524_527del): This variant has not been reported in the literature and is not present in large control databases. Evolutionary conservation and computational predictive tools for this variant are limited or unavailable. This variant is a deletion of 4 nucleotides at position 524 to 527 and creates a premature stop codon 7 amino acids downstream from this location which results in an absent or abnormal protein. Loss of function variants have been reported in association with disease for this gene (Villard 1997 PMID:9287230). In summary, this variant is classified as pathogenic.

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