NM_030621.4:c.3811C>T

HGVS Expressions

  • NG_016311.1:g.58838C>T
  • NM_030621.4:c.3811C>T
  • NP_085124.2:p.Leu1271Phe
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Genomic Location

chr14:95103585

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

579305

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.42LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B38' from family 15 in the publ...
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