ClinVar Miner

Submissions for variant NM_001457.4(FLNB):c.4377T>C (p.Val1459=)

gnomAD frequency: 0.00232  dbSNP: rs149921907
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000242047 SCV000307912 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000835394 SCV000977185 likely benign not provided 2021-10-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000835394 SCV001027779 benign not provided 2024-01-26 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000835394 SCV002049396 benign not provided 2021-10-08 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000835394 SCV004150385 likely benign not provided 2024-08-01 criteria provided, single submitter clinical testing FLNB: BP4, BP7

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