NM_007294.4:c.548-56del

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HGVS Expressions

  • NG_005905.2:g.120639del
  • NM_007294.4:c.548-56del

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43097346

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Deletion

dbSNP

1567804371

Clinvar

125894

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.12LebanonBenignBreast CancerJalkh et al, 2012 10 unrelated patients with breast cancer
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Contributors

  • Asha Deepthi: 03.06.2020

Edit History

  • Sayeeda Hana: 04.10.2020
  • Asha Deepthi: 07.06.2020
  • Asha Deepthi: 03.06.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.