NM_007294.4:c.4132G>A

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HGVS Expressions

  • NG_005905.2:g.126987G>A
  • NM_007294.4:c.4132G>A
  • NP_009225.1:p.Val1378Ile
  • NC_000017.11:g.43090997C>T

Associated Genes

Breast Cancer 1 Gene
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Clinvar Clinical Significance

Benign, Likely Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

28897690

Clinvar

55111

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.77LebanonUncertain SignificanceBreast CancerEl Saghir et al. 2015 Patient with stage III ductal carcinoma
114480.78LebanonUncertain SignificanceBreast CancerEl Saghir et al. 2015 Patient with stage IV ductal carcinoma
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Contributors

  • Asha Deepthi: 13.01.2021

Edit History

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