NM_007294.4:c.3367G>T

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HGVS Expressions

  • NG_005905.2:g.125820G>T
  • NM_007294.4:c.3367G>T
  • NP_009225.1:p.Asp1123Tyr
  • NC_000017.11:g.43092164C>A

Associated Genes

Breast Cancer 1 Gene
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Clinvar Clinical Significance

Likely Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

80356867

Clinvar

54860

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.75LebanonUncertain SignificanceBreast CancerEl Saghir et al. 2015 Patient with stage I 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.