ClinVar Miner

Submissions for variant NM_006361.6(HOXB13):c.519T>C (p.Ala173=)

dbSNP: rs1597933919
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003558615 SCV004300419 likely benign not provided 2023-07-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005249114 SCV005898685 benign Prostate cancer, hereditary, 9 2024-10-30 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.
Laboratory of Virology, Microbiology, Quality and Medical Biotechnologies, Faculty of Sciences and Techniques - Mohammedia, Hassan II University of Casablanca RCV000856127 SCV000994118 uncertain significance Prostate cancer, hereditary, 1 no assertion criteria provided clinical testing

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