ClinVar Miner

Submissions for variant NM_001614.5(ACTG1):c.1002G>C (p.Glu334Asp)

dbSNP: rs113262912
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000826155 SCV000967691 likely pathogenic Rare genetic deafness 2018-05-23 criteria provided, single submitter clinical testing The p.Glu334Asp variant in ACTG1 has been detected by our laborotory in one indi vidual with moderate sensorineural hearing loss who had a normal brain MRI at 1 year of age, and parental testing confirmed that the variant occured de novo in this individual. The variant was absent from large population studies. A differe nt change at this position (p.Glu334Gln) was reported as a de novo variant in an individual with Baraitser-Winter cerebrofrontofacial syndrome (BWCS) who presen ted with moderate sensorineural hearing loss along with other syndromic features of BWCS (Di Donato 2016). In addition, the glutamic acid residue at this positi on is well conserved across evolutionary distant species, and the ACTG1 gene is constrained for missense variation (z-score:5.13) in the ExAC general population cohort (Exome Aggregation Database: http://exac.broadinstitute.org). Taken toge ther, this information suggests that changes at this amino acid residue in ACTG1 may not be tolerated. In summary, although additional studies are required to fully establish its clinical significance, this variant is likely pathogenic. AC MG/AMP Criteria applied: PM2; PM5, PM6, PP2.

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