NM_153704.5:c.1675-109_1675-108insT

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  2. NM_153704.5:c.1675-109_1675-108insT

HGVS Expressions

  • NG_009190.1:g.45457_45458insT
  • NM_153704.5:c.1675-109_1675-108insT

Associated Genes

Transmembrane Protein 67
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Genomic Location

Chr8:93795300-93795301

CTGA Clinical Significance

Benign, Likely Benign

Variant Type

Insertion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
607361.5Tunisia2Benign, Likely BenignKhaddour et al. 2007 Individual is healthy
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Contributors

  • Sami Bizzari: 20.05.2020

Edit History

  • Rahila Mir: 07.02.2022
  • Sami Bizzari: 24.06.2020
  • Sami Bizzari: 23.06.2020
  • Sami Bizzari: 20.05.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.