ClinVar Miner

Submissions for variant NM_006846.4(SPINK5):c.962C>T (p.Pro321Leu)

dbSNP: rs1343893946
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003761207 SCV001559371 uncertain significance Ichthyosis linearis circumflexa 2023-08-17 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. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt SPINK5 protein function. ClinVar contains an entry for this variant (Variation ID: 1054710). This variant has not been reported in the literature in individuals affected with SPINK5-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.006%). This sequence change replaces proline, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 321 of the SPINK5 protein (p.Pro321Leu).

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