NM_007294.4:c.2612C>T

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HGVS Expressions

  • NG_005905.2:g.125065C>T
  • NM_007294.4:c.2612C>T
  • NP_009225.1:p.Pro871Leu

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43092919

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

799917

Clinvar

41812

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.23LebanonBenignBreast CancerJalkh et al, 2012 47 unrelated patients with breast cancer
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Contributors

  • Asha Deepthi: 03.06.2020

Edit History

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