NM_005591.4:c.1728A>T

HGVS Expressions

  • NG_007261.1:g.51601A>T
  • NM_005591.4:c.1728A>T
  • NP_005582.1:p.Arg576=
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Genomic Location

chr11:94447274

Clinvar Clinical Significance

Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

230008

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.50LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B46' from family 23 in the publ...
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