NM_000767.5:c.785A>G

HGVS Expressions

  • NG_007929.1:g.23060A>G
  • NM_000767.5:c.785A>G
  • NP_000758.1:p.Lys262Arg
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Genomic Location

chr19:41009358

Clinvar Clinical Significance

Drug Response

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

2279343

Clinvar

120171

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.2Lebanon0.29Drug ResponseBreast CancerOssaily and Zgheib. 2014 Patients with breast cancer
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