ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.*519C>T

dbSNP: rs886058228
Minimum review status: Collection method:
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000344612 SCV000442449 uncertain significance TP63-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000407099 SCV000442450 uncertain significance Cleft Lip +/- Cleft Palate, Autosomal Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000314402 SCV000442451 uncertain significance Ectrodactyly 2016-06-14 criteria provided, single submitter clinical testing

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