NM_181523.3:c.1346T>C

HGVS Expressions

  • NG_012849.2:g.83000T>C
  • NM_181523.3:c.1346T>C
  • NP_852664.1:p.Leu449Ser
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Genomic Location

chr5:68293755

CTGA Clinical Significance

Risk factor

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
167000.2Lebanon2Risk factorOvarian CancerMoussa et al, 2020
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