NM_031889.2:c.534+161_534+162insGAGA

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HGVS Expressions

  • NG_013024.1:g.12312_12313insGAGA
  • NM_031889.2:c.534+161_534+162insGAGA
  • NP_114095.2:p.?
  • NC_000004.12:g.70636055_70636056insGAGA

Associated Genes

Enamelin
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CTGA Clinical Significance

Benign

Variant Type

Insertion

dbSNP

201212976

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
104500.1Lebanon1BenignHart et al., 2003 Benign variants seen in family, but not ...
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Contributors

  • Pratibha Nair: 08.10.2018

Edit History

  • Pratibha Nair: 08.11.2022
  • Rahila Mir: 07.02.2022
  • Sayeeda Hana: 17.09.2020
  • Pratibha Nair: 06.01.2019
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.