ClinVar Miner

Submissions for variant NM_023110.3(FGFR1):c.181G>A (p.Val61Met)

gnomAD frequency: 0.00003  dbSNP: rs762089291
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001928973 SCV002204292 uncertain significance Hypogonadotropic hypogonadism 2 with or without anosmia; Pfeiffer syndrome 2023-07-19 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt FGFR1 protein function. ClinVar contains an entry for this variant (Variation ID: 1423631). This missense change has been observed in individual(s) with craniosynostosis (PMID: 29168297). This variant is present in population databases (rs762089291, gnomAD 0.002%). This sequence change replaces valine, which is neutral and non-polar, with methionine, which is neutral and non-polar, at codon 61 of the FGFR1 protein (p.Val61Met).

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