ClinVar Miner

Submissions for variant NM_032638.5(GATA2):c.1027A>T (p.Arg343Ter)

dbSNP: rs1313081073
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000984817 SCV001132698 likely pathogenic not provided 2018-08-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001062521 SCV001227328 pathogenic Deafness-lymphedema-leukemia syndrome; Monocytopenia with susceptibility to infections 2019-06-21 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in GATA2 are known to be pathogenic (PMID: 21670465, 23223431). This variant has not been reported in the literature in individuals with GATA2-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Arg343*) in the GATA2 gene. It is expected to result in an absent or disrupted protein product.

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