ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.965G>C (p.Arg322Thr)

gnomAD frequency: 0.00005  dbSNP: rs144557211
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
Revvity Omics, Revvity RCV003137276 SCV003827257 uncertain significance not provided 2020-11-04 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV003137276 SCV004225943 uncertain significance not provided 2022-03-25 criteria provided, single submitter clinical testing BP4, PM2

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