ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.706G>A (p.Asp236Asn)

dbSNP: rs1860544115
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001209820 SCV001381271 uncertain significance PTEN hamartoma tumor syndrome 2019-08-28 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. This variant has been reported to have conflicting or insufficient data to determine the effect on PTEN protein function (PMID: 29706350). This variant has not been reported in the literature in individuals with PTEN-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces aspartic acid with asparagine at codon 236 of the PTEN protein (p.Asp236Asn). The aspartic acid residue is moderately conserved and there is a small physicochemical difference between aspartic acid and asparagine.

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