ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12758_1965-12753dup

dbSNP: rs864622087
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000206416 SCV000259302 uncertain significance Pancreatic adenocarcinoma 2015-07-06 criteria provided, single submitter clinical testing In summary, this is a novel change with uncertain impact on protein function. There is no indication that this variant causes disease, but the evidence is insufficient at this time to prove that conclusively. Therefore, it has been classified as a Variant of Uncertain Significance. This variant has not been published in the literature and is not present in population databases. This sequence change inserts 6 nucleotides in exon 2 of the PALLD mRNA (c.273_278dup). This leads to the insertion of 2 amino acid residues in the PALLD protein (p.Pro93_Pro94dup). These additional amino acid residues extend a 7 proline repeat region of the PALLD protein, but otherwise preserves the integrity of the reading frame.

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