NM_025114.4:c.6011+160G>A

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HGVS Expressions

  • NG_008417.2:g.76083G>A
  • NM_025114.4:c.6011+160G>A
  • NC_000012.12:g.88071134C>T

Associated Genes

Centrosomal Protein 290
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CTGA Clinical Significance

Benign

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615982.3Saudi Arabia1BenignAbu-Safieh et al. 2012; Abu Safieh et al. 2010 "BBS-F013-A" in the publication
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Contributors

  • Sayeeda Hana: 13.07.2022

Edit History

  • Sayeeda Hana: 21.07.2022
  • Sayeeda Hana: 13.07.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.