ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.*235_*238del

dbSNP: rs886058225
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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 RCV000301990 SCV000442431 uncertain significance Ectrodactyly 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000366302 SCV000442432 uncertain significance TP63-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000271698 SCV000442433 uncertain significance Cleft Lip +/- Cleft Palate, Autosomal Dominant 2016-06-14 criteria provided, single submitter clinical testing

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