NM_004360.5:c.1774G>A

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  2. NM_004360.5:c.1774G>A

HGVS Expressions

  • NG_008021.1:g.89772G>A
  • NM_004360.5:c.1774G>A
  • NP_004351.1:p.Ala592Thr

Associated Genes

Cadherin 1
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Genomic Location

chr16:68822063

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

dbSNP

35187787

Clinvar

41783

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.33LebanonLikely PathogenicBreast CancerJalkh et al, 2017 Patient 'B27' from family 8 in the publi...
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Contributors

  • Asha Deepthi: 16.09.2020

Edit History

  • Asha Deepthi: 30.09.2020
  • Asha Deepthi: 16.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.