ClinVar Miner

Submissions for variant NM_004371.4(COPA):c.3259A>T (p.Met1087Leu)

dbSNP: rs2101819861
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV001807867 SCV002058116 uncertain significance Systemic autoinflammation no assertion criteria provided clinical testing

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