ClinVar Miner

Submissions for variant NM_006185.4(NUMA1):c.2937T>C (p.Asn979=)

gnomAD frequency: 0.00416  dbSNP: rs142372284
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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 RCV000973476 SCV001121235 benign not provided 2018-07-23 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002503096 SCV002813095 likely benign Acute promyelocytic leukemia 2022-04-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000973476 SCV005232494 benign not provided criteria provided, single submitter not provided

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