ClinVar Miner

Submissions for variant NM_001012759.3(CTU2):c.1120G>T (p.Gly374Cys)

dbSNP: rs61730418
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000961366 SCV001108409 benign not provided 2024-12-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000961366 SCV005249711 benign not provided criteria provided, single submitter not provided

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