ClinVar Miner

Submissions for variant NM_000755.5(CRAT):c.871A>G (p.Thr291Ala)

gnomAD frequency: 0.00155  dbSNP: rs145822836
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000999240 SCV001155763 uncertain significance not provided 2016-06-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000999240 SCV001730051 benign not provided 2024-01-22 criteria provided, single submitter clinical testing

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