ClinVar Miner

Submissions for variant NM_006019.4(TCIRG1):c.1583G>C (p.Ser528Thr)

gnomAD frequency: 0.00003  dbSNP: rs555362865
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000727901 SCV000855407 uncertain significance not provided 2017-07-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000727901 SCV002475274 likely benign not provided 2024-05-10 criteria provided, single submitter clinical testing

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