ClinVar Miner

Submissions for variant NM_014339.7(IL17RA):c.996_997delinsCT (p.Val333Leu)

dbSNP: rs2061413124
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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 RCV001303597 SCV001492846 uncertain significance Immunodeficiency 51 2022-10-28 criteria provided, single submitter clinical testing 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. ClinVar contains an entry for this variant (Variation ID: 1006539). This variant has not been reported in the literature in individuals affected with IL17RA-related conditions. Information on the frequency of this variant in the gnomAD database is not available, as this variant may be reported differently in the database. This variant, c.996_997delinsCT, is a complex sequence change that results in the deletion of valine and insertion of leucine amino acid(s) in the IL17RA protein (p.Val333Leu).

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