ClinVar Miner

Submissions for variant NM_003200.5(TCF3):c.1291G>A (p.Gly431Ser)

gnomAD frequency: 0.08952  dbSNP: rs1052692
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001517623 SCV001726158 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001517623 SCV001839404 benign not provided 2020-04-01 criteria provided, single submitter clinical testing
Dept. of Cytogenetics, ICMR- National Institute of Immunohaematology RCV002284220 SCV002573662 likely pathogenic Myeloproliferative neoplasm, unclassifiable 2022-08-25 criteria provided, single submitter clinical testing

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