NM_000213.5:c.2855del

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HGVS Expressions

  • NG_007372.2:g.26197del
  • NM_000213.5:c.2855del
  • NP_000204.3:p.Pro952LeufsTer28
  • NC_000017.11:g.75742654del

Associated Genes

Integrin, Beta-4
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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
147557.G.1Saudi Arabia2Monies et al. 2017 Couple with heterozygous variants in ITG...
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Contributors

  • Asha Deepthi: 15.11.2024

Edit History

  • Asha Deepthi: 15.11.2024
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.