NM_007294.4:c.4985T>C

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HGVS Expressions

  • NG_005905.2:g.147055T>C
  • NM_007294.4:c.4985T>C
  • NP_009225.1:p.Phe1662Ser
  • NC_000017.11:g.43070929A>G

Associated Genes

Breast Cancer 1 Gene
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Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

28897695

Clinvar

55339

Epidemiology in the Arab World

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Contributors

  • Asha Deepthi: 13.01.2021

Edit History

  • Asha Deepthi: 13.01.2021
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© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.