NM_001460.5:c.337del

HGVS Expressions

  • NM_001460.5:c.337del
  • NP_001451.2:p.Ser112_Val113insTer
  • NC_000001.11:g.171196664del
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Drug Response

Variant Type

Deletion

Clinvar

402870

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.5LebanonDrug ResponseBreast CancerAwada et al. 2013 Case-control study observed 12 SNPs to b...
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