NM_000455.5:c.375-1C>T

HGVS Expressions

  • NG_007460.2:g.34917C>T
  • NM_000455.5:c.375-1C>T
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Genomic Location

chr19:1219323

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
114480.31LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B25' from family 6 in the publi...
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