ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1964+44317_1964+44318inv

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001294785 SCV001483679 uncertain significance Pancreatic adenocarcinoma 2023-12-16 criteria provided, single submitter clinical testing This variant occurs in a non-coding region of the PALLD gene. It does not change the encoded amino acid sequence of the PALLD protein. 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 has not been reported in the literature in individuals affected with PALLD-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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.

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