NM_007294.4:c.3526G>A

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HGVS Expressions

  • NG_005905.2:g.125979G>A
  • NM_007294.4:c.3526G>A
  • NP_009225.1:p.Val1176Ile

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43092005

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

777796838

Clinvar

565640

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.4LebanonJalkh et al, 2012
114480.76LebanonUncertain SignificanceBreast CancerEl Saghir et al. 2015 Patient with stage II ductal carcinoma
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Contributors

  • Asha Deepthi: 03.06.2020

Edit History

  • Asha Deepthi: 13.01.2021
  • Asha Deepthi: 07.06.2020
  • Asha Deepthi: 03.06.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.