NM_002878.3:c.494G>A

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HGVS Expressions

  • NG_031858.1:g.18402G>A
  • NM_002878.3:c.494G>A
  • NP_002869.3:p.Arg165Gln

Associated Genes

RAD51 Paralog D
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Genomic Location

chr17:35106468

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

4796033

Clinvar

142159

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.31LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B25' from family 6 in the publi...
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Contributors

  • Asha Deepthi: 13.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 30.09.2020
  • Asha Deepthi: 13.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.