ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.*45C>T (rs34057105)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000252369 SCV000309783 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000293324 SCV000442422 benign TP63-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000348286 SCV000442423 benign Cleft Lip +/- Cleft Palate, Autosomal Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000375399 SCV000442424 benign Ectrodactyly 2016-06-14 criteria provided, single submitter clinical testing

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