NM_032444.4:c.1919C>A

HGVS Expressions

  • NG_028123.1:g.20427C>A
  • NM_032444.4:c.1919C>A
  • NP_115820.2:p.Thr640Asn
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Genomic Location

chr16:3596158

Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

962446

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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