NM_000367.4:c.460G>A

HGVS Expressions

  • NG_012137.2:g.21147G>A
  • NM_000367.4:c.460G>A
  • NP_001333746.1:p.Ala154Thr
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Genomic Location

chr6:18138997

Clinvar Clinical Significance

Drug Response

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

1800460

Clinvar

37126

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
610460.1Lebanon1Drug ResponseThiopurines, Poor Metabolism of, 1Zgheib et al. 2017
610460.2Lebanon1Drug ResponseThiopurines, Poor Metabolism of, 1Zgheib et al. 2017
610460.3Lebanon1Drug ResponseThiopurines, Poor Metabolism of, 1Zgheib et al. 2017
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