NM_000767.5:c.1459C>A

HGVS Expressions

  • NG_007929.1:g.30512C>A
  • NM_000767.5:c.1459C>A
  • NP_000758.1:p.Arg487Ser
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Genomic Location

chr19:41016810

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

3211371

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.2Lebanon0.07Drug ResponseBreast CancerOssaily and Zgheib. 2014 Patients with breast cancer
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