NM_004333.6:c.1798delinsTACA

HGVS Expressions

  • NG_007873.3:g.176428delinsTACA
  • NM_004333.6:c.1798delinsTACA
  • NP_004324.2:p.Val600TyrMet
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Genomic Location

chr7:140753337

Variant Type

Indel

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
211980.3LebanonLung CancerEl Karak et al, 2015 BRAF mutation observed in a non-small-ce...
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