ClinVar Miner

Submissions for variant NM_030667.3(PTPRO):c.1327G>A (p.Val443Ile)

gnomAD frequency: 0.00942  dbSNP: rs71459181
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000953461 SCV001100034 benign not provided 2023-12-11 criteria provided, single submitter clinical testing
GeneDx RCV000953461 SCV002005944 likely benign not provided 2023-02-18 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Breakthrough Genomics, Breakthrough Genomics RCV000953461 SCV005215995 likely benign not provided criteria provided, single submitter not provided

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