NM_004580.5:c.17A>G

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HGVS Expressions

  • NG_009103.1:g.59886A>G
  • NM_004580.5:c.17A>G
  • NP_899059.1:p.Tyr6Cys
  • NC_000015.10:g.55234918T>C

Associated Genes

Ras-Associated Protein RAB27A
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

145253993

Clinvar

536463

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.18Lebanon1Uncertain SignificanceUmar et al, 2020
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Contributors

  • Sayeeda Hana: 03.02.2021

Edit History

  • Sayeeda Hana: 15.02.2021
  • Sayeeda Hana: 03.02.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.