ClinVar Miner

Submissions for variant NM_003467.3(CXCR4):c.1042A>G (p.Ser348Gly)

dbSNP: rs1573613407
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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 RCV001934498 SCV002134998 uncertain significance Warts, hypogammaglobulinemia, infections, and myelokathexis 2023-08-04 criteria provided, single submitter clinical testing This variant is not present in population databases (gnomAD no frequency). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be tolerated. ClinVar contains an entry for this variant (Variation ID: 1362599). This variant has not been reported in the literature in individuals affected with CXCR4-related conditions. This sequence change replaces serine, which is neutral and polar, with glycine, which is neutral and non-polar, at codon 348 of the CXCR4 protein (p.Ser348Gly).

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