ClinVar Miner

Submissions for variant NM_006361.6(HOXB13):c.147C>T (p.Ala49=)

dbSNP: rs2143074721
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002184789 SCV002346846 likely benign not provided 2024-10-29 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005247390 SCV005895405 benign Prostate cancer, hereditary, 9 2024-10-29 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.

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