ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.459G>A (p.Lys153=)

gnomAD frequency: 0.00002  dbSNP: rs766153167
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000645525 SCV000767271 likely benign Multiple endocrine neoplasia type 4 2023-12-05 criteria provided, single submitter clinical testing
Ambry Genetics RCV001022762 SCV001184533 likely benign Hereditary cancer-predisposing syndrome 2019-07-30 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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