ClinVar Miner

Submissions for variant NM_001453.3(FOXC1):c.957del (p.Ser320fs)

dbSNP: rs1241813534
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000646228 SCV000767988 pathogenic Axenfeld-Rieger syndrome type 3 2023-11-19 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Ser320Argfs*81) in the FOXC1 gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 234 amino acid(s) of the FOXC1 protein. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This premature translational stop signal has been observed in individual(s) with Axenfeld-Rieger syndrome (Invitae). In at least one individual the variant was observed to be de novo. ClinVar contains an entry for this variant (Variation ID: 537391). For these reasons, this variant has been classified as Pathogenic.

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