NM_000543.4:c.1244C>T

HGVS Expressions

  • NG_011780.1:g.7944C>T
  • NM_000543.4:c.1244C>T
  • NP_000534.3:p.Ala415Val
  • NC_000011.10:g.6393368C>T
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CTGA Clinical Significance

Likely Pathogenic, Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
607616.1United Arab Emirates2Likely PathogenicNiemann-Pick Disease, Type BBen-Rebeh et al. 2012
607616.2United Arab Emirates2PathogenicNiemann-Pick Disease, Type BAl-Jasmi et al. 2013
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