ClinVar Miner

Submissions for variant NM_021939.4(FKBP10):c.124G>T (p.Glu42Ter)

dbSNP: rs2144041488
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
3billion RCV002250878 SCV002521057 pathogenic Bruck syndrome 1 2022-05-22 criteria provided, single submitter clinical testing The variant is not observed in the gnomAD v2.1.1 dataset. Stop-gained (nonsense): predicted to result in a loss or disruption of normal protein function through nonsense-mediated decay (NMD) or protein truncation. Multiple pathogenic variants are reported downstream of the variant. This variant is shared with the similiarly affected sibling (3billion dataset). The variant has been reported to be associated with FKBP10 related disorder (3billion dataset). Therefore, this variant is classified as pathogenic according to the recommendation of ACMG/AMP guideline.

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