NM_001904.4:c.2315A>G

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HGVS Expressions

  • NG_013302.2:g.44861A>G
  • NM_001904.4:c.2315A>G
  • NP_001895.1:p.Asn772Ser

Associated Genes

Catenin, Beta-1
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Genomic Location

chr3:41239311

Clinvar Clinical Significance

Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

138501547

Clinvar

726679

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.54LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B50' from family 25 in the publ...
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Contributors

  • Asha Deepthi: 29.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 29.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.