NM_152383.5:c.1651_1652insGGG

HGVS Expressions

  • NG_032572.1:g.306850_306851insGGG
  • NM_152383.5:c.1651_1652insGGG
  • NP_689596.4:p.Leu551delinsTrpVal
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Genomic Location

chr2:232263432-232263433

CTGA Clinical Significance

Uncertain Significance

Variant Type

Insertion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.52LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B48' from family 38 in the publ...
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