NM_007294.4:c.1771A>G

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  2. NM_007294.4:c.1771A>G

HGVS Expressions

  • NG_005905.2:g.124224A>G
  • NM_007294.4:c.1771A>G
  • NP_009225.1:p.Ile591Val
  • NC_000017.11:g.43093760T>C

Associated Genes

Breast Cancer 1 Gene
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Clinvar Clinical Significance

Benign, Likely Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

1064795358

Clinvar

421781

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
176807.1United Arab EmiratesUncertain SignificanceProstate CancerAl-Ali et al. 2023
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Contributors

  • Pratibha Nair: 23.01.2024

Edit History

  • Pratibha Nair: 23.01.2024
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.