NM_032444.4:c.1837C>T

HGVS Expressions

  • NG_028123.1:g.20345C>T
  • NM_032444.4:c.1837C>T
  • NP_115820.2:p.Gln613Ter
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Genomic Location

chr16:3596240

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
114480.26LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B19' from family 1 in the publi...
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