NM_000797.4:c.155dup

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  2. NM_000797.4:c.155dup

HGVS Expressions

  • NG_021241.1:g.5155dup
  • NM_000797.4:c.155dup
  • NP_000788.2:p.Asn52fs

Associated Genes

Dopamine Receptor D4
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Genomic Location

chr11:637459

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Duplication

dbSNP

750696928

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
143465.1Lebanon1Likely PathogenicAttention Deficit-Hyperactivity DisorderJalkh et al. 2019
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Contributors

  • Pratibha Nair: 15.11.2020

Edit History

  • Rahila Mir: 14.02.2022
  • Pratibha Nair: 15.11.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.