NM_001080125.2:c.*429A>G

HGVS Expressions

  • NG_007497.1:g.58566A>G
  • NM_001080125.2:c.*429A>G
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Genomic Location

chr2:201287023

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

333519

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.26LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B19' from family 1 in the publi...
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