ClinVar Miner

Submissions for variant NM_139315.3(TAF6):c.76A>T (p.Met26Leu)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003423663 SCV004162636 likely benign not provided 2022-05-01 criteria provided, single submitter clinical testing TAF6: BS2
Labcorp Genetics (formerly Invitae), Labcorp RCV003423663 SCV004312803 benign not provided 2024-01-02 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003954198 SCV004775859 benign TAF6-related disorder 2020-01-21 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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