NM_000044.3:c.1617-3C>G

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HGVS Expressions

  • NG_009014.2:g.104222C>G
  • NM_000044.3:c.1617-3C>G
  • NP_000035.2:p.?
  • NC_000023.11:g.67643253C>G

Associated Genes

Androgen Receptor
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
300068.6.1Lebanon1Likely PathogenicAndrogen Insensitivity SyndromeGannagé-Yared et al. 2005 Sibling of 300068.6.2
300068.6.2Lebanon1Likely PathogenicAndrogen Insensitivity SyndromeGannagé-Yared et al. 2005 Sibling of 300068.6.1
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Contributors

  • Pratibha Nair: 26.06.2018

Edit History

  • Pratibha Nair: 08.11.2022
  • Rahila Mir: 10.02.2022
  • Pratibha Nair: 09.06.2021
  • Pratibha Nair: 31.12.2018
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.