NM_001394783.1:c.554_585del

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HGVS Expressions

  • NG_012637.1:g.8315_8346del
  • NM_001394783.1:c.554_585del
  • NP_001381712.1:p.Ser185IlefsTer32
  • NC_000003.12:g.46373456_46373487del

Associated Genes

Chemokine, CC Motif, Receptor 5
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Clinvar Clinical Significance

Benign, Protective, Risk factor

CTGA Clinical Significance

Uncertain Significance

Variant Type

Deletion

dbSNP

333

Clinvar

8184

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
601373.1United Arab Emirates10.002Uncertain SignificanceAl-Jaberi et al. 2013 Healthy adult with heterozygous CCR5D32 ...
601373.G.1Tunisia40.013Uncertain SignificanceAl-Jaberi et al. 2013 Four healthy adults with heterozygous CC...
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Contributors

  • Asha Deepthi: 04.04.2022

Edit History

  • Asha Deepthi: 05.12.2022
  • Asha Deepthi: 04.04.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.