NM_004360.5:c.160A>G

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HGVS Expressions

  • NG_008021.1:g.6117A>G
  • NM_004360.5:c.160A>G
  • NP_004351.1:p.Arg54Gly

Associated Genes

Cadherin 1
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Genomic Location

chr16:68738408

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

587781329

Clinvar

140862

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.62LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'D12' from family 33 in the publ...
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Contributors

  • Asha Deepthi: 16.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 16.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.