ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.559+8G>A (rs775915220)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000726139 SCV000342331 uncertain significance not provided 2016-05-27 criteria provided, single submitter clinical testing
Invitae RCV000633405 SCV000754627 likely benign Li-Fraumeni syndrome 2017-10-24 criteria provided, single submitter clinical testing
PreventionGenetics RCV000253181 SCV000305115 likely benign not specified criteria provided, single submitter clinical testing

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