NM_001351.4:c.571-1G>C

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HGVS Expressions

  • NG_023329.1:g.15916G>C
  • NM_001351.4:c.571-1G>C
  • NC_000003.12:g.16594584C>G

Associated Genes

Deleted in Azoospermia-Like
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

dbSNP

1694568951

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
258150.6Saudi Arabia2Likely PathogenicSpermatogenic Failure 1Alhathal et al. 2020
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Contributors

  • Pratibha Nair: 16.03.2023

Edit History

  • Pratibha Nair: 16.03.2023
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.