NM_001113378.1:c.1289_1290del

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HGVS Expressions

  • NG_011736.1:g.37925_37926del
  • NM_001113378.1:c.1289_1290del
  • NP_001106849.1:p.Phe430Ter
  • NC_000015.10:g.89276887_89276888del

Associated Genes

FANCI Gene
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Variant Type

Deletion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605988.GUnited Arab EmiratesAlmarzooqi et al. 2021 Study on symptomatic and asymptomatic Em...
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Contributors

  • Sami Bizzari: 20.07.2022

Edit History

  • Sami Bizzari: 26.07.2022
  • Sami Bizzari: 20.07.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.