ClinVar Miner

Submissions for variant NM_032977.4(CASP10):c.1296C>T (p.Ala432=)

gnomAD frequency: 0.00298  dbSNP: rs41331850
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001796766 SCV000765624 benign Autoimmune lymphoproliferative syndrome type 2A 2024-01-11 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001816600 SCV002066483 benign not specified 2021-07-27 criteria provided, single submitter clinical testing

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