ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.*2544del

dbSNP: rs201395656
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000281489 SCV000442551 benign Ectrodactyly 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000340710 SCV000442552 benign TP63-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000400398 SCV000442553 benign Cleft Lip +/- Cleft Palate, Autosomal Dominant 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001718733 SCV001948478 benign not provided 2021-06-04 criteria provided, single submitter clinical testing

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