NM_024426.6:c.1250G>T

HGVS Expressions

  • NG_009272.1:g.44271G>T
  • NM_024426.6:c.1250G>T
  • NP_077744.4:p.Ser417Ile

Associated Genes

WT1 Transcription Factor
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Genomic Location

chr11:32396271

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
256370.1Lebanon1PathogenicNephrotic Syndrome, Type 4Nair et al. 2018
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