ClinVar Miner

Submissions for variant NM_006361.6(HOXB13):c.333G>T (p.Ala111=)

dbSNP: rs757423683
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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 RCV002212072 SCV002357976 likely benign not provided 2023-12-03 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005247414 SCV005895428 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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