NM_002691.4:c.2793G>C

HGVS Expressions

  • NG_033800.1:g.36477G>C
  • NM_002691.4:c.2793G>C
  • NP_002682.2:p.Lys931Asn
  • NC_000019.10:g.50415799G>C
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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
114480.48LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B44' from family 21 in the publ...
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