ClinVar Miner

Submissions for variant NM_003268.6(TLR5):c.2537A>G (p.Asp846Gly)

gnomAD frequency: 0.00773  dbSNP: rs5744177
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia RCV000238959 SCV000297139 benign not specified 2015-07-30 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003417853 SCV004125663 likely benign not provided 2023-03-01 criteria provided, single submitter clinical testing TLR5: BP4, BS2
Breakthrough Genomics, Breakthrough Genomics RCV003417853 SCV005281193 benign not provided criteria provided, single submitter not provided

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