NM_004456.5:c.349C>T

HGVS Expressions

  • NG_032043.1:g.56702C>T
  • NM_004456.5:c.349C>T
  • NP_004447.2:p.Gln117Ter
  • NC_000007.14:g.148832648A>G
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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
114480.30LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B24' from family 5 in the publi...
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