NM_001166271.3:c.2667+66T>C

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  2. NM_001166271.3:c.2667+66T>C

HGVS Expressions

  • NM_001166271.3:c.2667+66T>C
  • NP_001159743.1:p.?
  • NC_000013.11:g.24287016T>C

Associated Genes

Spermatogenesis-Associated Protein 13
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

908890896

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
220290.G.11.1United Arab Emirates6Uncertain SignificanceMahfood et al. 2021 3 siblings (2 male, 1 female) with a mol...
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Contributors

  • Sami Bizzari: 22.02.2022

Edit History

  • Sami Bizzari: 22.02.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.