NM_005432.4:c.260C>T

HGVS Expressions

  • NG_011516.1:g.13338C>T
  • NM_005432.4:c.260C>T
  • NP_005423.1:p.Pro87Leu
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Genomic Location

chr14:103707149

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.53LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B49' from family 24 in the publ...
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