NM_007294.3:c.441+18CTT[6]

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  2. NM_007294.3:c.441+18CTT[6]

HGVS Expressions

  • NG_005905.2:g.113880CTT[6]
  • NM_007294.3:c.441+18CTT[6]
  • NC_000017.11:g.43104086GAA[6]

Associated Genes

Breast Cancer 1 Gene
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Clinvar Clinical Significance

Benign

Variant Type

Deletion

dbSNP

147856441

Clinvar

225704

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.10LebanonBreast CancerJalkh et al, 2012 6 unrelated patients with breast cancer
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Contributors

  • Asha Deepthi: 03.06.2020

Edit History

  • Asha Deepthi: 26.09.2021
  • Asha Deepthi: 07.06.2020
  • Asha Deepthi: 03.06.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.