ClinVar Miner

Submissions for variant NM_002354.2(EPCAM):c.93C>G (p.Asn31Lys) (rs555329870)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000168222 SCV000218890 likely benign not provided 2016-12-08 criteria provided, single submitter clinical testing
St. Jude Clinical Genomics Lab, St. Jude Children's Research Hospital RCV000761123 SCV000891039 uncertain significance Ewing sarcoma of soft tissue 2016-12-27 criteria provided, single submitter clinical testing
Invitae RCV001432261 SCV001635026 likely benign Hereditary nonpolyposis colorectal neoplasms 2016-11-13 criteria provided, single submitter clinical testing
Ding PR Lab,Sun Yat-sen University Cancer Center RCV001093678 SCV001250859 uncertain significance Lynch syndrome I no assertion criteria provided clinical testing

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