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Evaluation of Suspected Autosomal Alport Syndrome Synonymous Variants.

Rini RossantiTomoko HorinouchiTomohiko YamamuraChina NaganoNana SakakibaraShinya IshikoYuya AotoAtsushi KondoSadayuki NagaiEri OkadaShingo IshimoriHiroaki NagaseSatoshi MatsuiKeiichi TamagakiYoshifumi UbaraMasahiko NagahamaYuko ShimaKoichi NakanishiTakeshi NinchojiMasafumi MatsuoKazumoto IijimaKandai Nozu
Published in: Kidney360 (2021)
This study highlights the pitfalls of classifying the functional consequences of variants by a simple approach. Certain synonymous variants, although they do not alter the amino acid sequence of the encoded protein, can dramatically affect pre-mRNA splicing, as shown in two of our patients. Our findings indicate that transcript analysis should be carried out to evaluate synonymous variants detected in patients with autosomal dominant Alport syndrome.
Keyphrases
  • copy number
  • amino acid
  • end stage renal disease
  • ejection fraction
  • chronic kidney disease
  • case report
  • binding protein
  • dna methylation
  • small molecule
  • rna seq