ClinVar Miner

Submissions for variant NM_001278495.2(NUTM2B):c.2027T>C (p.Met676Thr)

gnomAD frequency: 0.01752  dbSNP: rs61863495
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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
Breakthrough Genomics, Breakthrough Genomics RCV001573518 SCV005318236 benign not provided criteria provided, single submitter not provided
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001573518 SCV001799514 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001727888 SCV001973533 benign not specified no assertion criteria provided clinical testing

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