NM_005475.3:c.784T>A

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  2. NM_005475.3:c.784T>A

HGVS Expressions

  • NG_021216.1:g.45857T>A
  • NM_005475.3:c.784T>A
  • NP_001278353.1:p.Trp60Arg
  • NC_000012.12:g.111446804T>A

Associated Genes

SH2B Adaptor Protein 3
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

3184504

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608446.G.1LebanonBenignSaade et al. 2011 Study of 2002 Lebanese subjects to asses...
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Contributors

  • Sayeeda Hana: 24.03.2021

Edit History

  • Rahila Mir: 22.02.2022
  • Sayeeda Hana: 29.03.2021
  • Sayeeda Hana: 24.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.