ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.639A>G (p.Arg213=) (rs1800372)

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Total submissions: 13
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000755410 SCV000605419 benign not provided 2017-05-02 criteria provided, single submitter clinical testing
Ambry Genetics RCV000162403 SCV000212733 benign Hereditary cancer-predisposing syndrome 2014-11-18 criteria provided, single submitter clinical testing
Color RCV000162403 SCV000537359 benign Hereditary cancer-predisposing syndrome 2015-03-31 criteria provided, single submitter clinical testing
Counsyl RCV000203086 SCV000488466 benign Li-Fraumeni syndrome 1 2016-04-08 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000203086 SCV000733709 benign Li-Fraumeni syndrome 1 no assertion criteria provided clinical testing
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia RCV000203086 SCV000257782 benign Li-Fraumeni syndrome 1 2015-07-10 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000036533 SCV000111073 benign not specified 2015-03-27 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000206135 SCV000407069 likely benign Li-Fraumeni syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000206135 SCV000262407 benign Li-Fraumeni syndrome 2017-08-18 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000036533 SCV000060188 benign not specified 2008-09-15 no assertion criteria provided clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000036533 SCV000692079 benign not specified no assertion criteria provided clinical testing
PreventionGenetics RCV000036533 SCV000305116 benign not specified criteria provided, single submitter clinical testing
True Health Diagnostics RCV000162403 SCV000788225 likely benign Hereditary cancer-predisposing syndrome 2017-12-08 no assertion criteria provided clinical testing

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