NM_004484.4:c.79_81CCG[6]

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HGVS Expressions

  • NG_009286.1:g.5269_5271CCG[6]
  • NM_004484.4:c.79_81CCG[6]
  • NP_004475.1:p.Pro31dup

Associated Genes

Glypican 3
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Genomic Location

chrX:133985357-133985359

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Duplication

dbSNP

749104500

Clinvar

408895

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.44LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B40' from family 17 in the publ...
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Contributors

  • Asha Deepthi: 30.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Sayeeda Hana: 05.10.2020
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 30.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.