NM_004629.2:c.452T>A

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  2. NM_004629.2:c.452T>A

HGVS Expressions

  • NG_007312.1:g.6818T>A
  • NM_004629.2:c.452T>A
  • NP_004620.1:p.Leu151Ter

Associated Genes

FANCG Gene
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Genomic Location

chr9:35078199

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
614082.1Lebanon2PathogenicFanconi Anemia, Complementation Group GFarah et al. 2020
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Contributors

  • Pratibha Nair: 22.09.2020

Edit History

  • Rahila Mir: 17.02.2022
  • Pratibha Nair: 22.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.