ClinVar Miner

Submissions for variant NM_000110.4(DPYD):c.1925T>C (p.Met642Thr)

dbSNP: rs2101564724
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
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579723 SCV001808256 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001579723 SCV001965074 uncertain significance not provided no assertion criteria provided clinical testing

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