NM_033084.4:c.1275_1278+5delinsTTTAT

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HGVS Expressions

  • NM_033084.4:c.1275_1278+5delinsTTTAT
  • NP_149075.2:p.Tyr425_Leu426delins
  • NC_000003.12:g.10046720_10046728delinsTTTAT

Associated Genes

FANCD2 Gene
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Variant Type

Indel

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.