ClinVar Miner

Submissions for variant NM_207037.2(TCF12):c.2006G>T (p.Cys669Phe)

dbSNP: rs1597901046
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GenomeConnect, ClinGen RCV000844962 SCV000986787 not provided not provided no assertion provided phenotyping only Variant interpretted as Likely pathogenic and reported on 03/01/2017 by GTR ID 26957. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.

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