NM_007294.4:c.4654T>C

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HGVS Expressions

  • NG_005905.2:g.143632T>C
  • NM_007294.4:c.4654T>C
  • NP_009225.1:p.Tyr1552His

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43074352

Clinvar Clinical Significance

Likely Benign

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

1265352633

Clinvar

433716

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.6LebanonLikely BenignBreast CancerJalkh et al, 2012
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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.