NM_004273.5:c.141G>C

HGVS Expressions

  • NG_012635.1:g.47811G>A
  • NM_004273.5:c.141G>C
  • NP_004264.2:p.Arg47Ser
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Genomic Location

chr10:72007172

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
143095.3.01Lebanon1PathogenicSpondyloepiphyseal Dysplasia with Congenital Joint DislocationsUnger et al. 2010
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