NM_000754.3:c.472G>A

HGVS Expressions

  • NG_011526.1:g.27009G>A
  • NM_000754.3:c.472G>A
  • NP_000745.1:p.Val158Met
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Genomic Location

chr22:19963748

Clinvar Clinical Significance

Drug Response

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

4680

Clinvar

17591

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
600018.G.1.2Lebanon420.49Drug ResponseHajj et al. 2017 From a study of 84 cancer patients
600018.G.1.3Lebanon400.49Drug ResponseHajj et al. 2017 From a study of 84 cancer patients
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