ClinVar Miner

Submissions for variant NM_004357.5(CD151):c.252G>T (p.Lys84Asn)

gnomAD frequency: 0.00336  dbSNP: rs116211118
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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 RCV002190023 SCV002353978 benign not provided 2024-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002190023 SCV005319655 benign not provided criteria provided, single submitter not provided
Mayo Clinic Laboratories, Mayo Clinic RCV002190023 SCV005412268 uncertain significance not provided 2023-10-04 criteria provided, single submitter clinical testing

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