NM_024675.4:c.3464C>G

HGVS Expressions

  • NG_007406.1:g.42802C>G
  • NM_024675.4:c.3464C>G
  • NP_078951.2:p.Ser1155Cys
  • NC_000016.10:g.23603556G>C
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

402308

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.112United Arab EmiratesNANAUncertain SignificanceBreast CancerDeuitch et al. 2020 Patient was also identified with a 'like...
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