NM_032444.4:c.3337G>C

HGVS Expressions

  • NG_028123.1:g.26284G>C
  • NM_032444.4:c.3337G>C
  • NP_115820.2:p.Gly1113Arg
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Genomic Location

chr16:3590301

Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

1038292

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.45LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B41' from family 18 in the publ...
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