NM_002876.3:c.376G>A

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  2. NM_002876.3:c.376G>A

HGVS Expressions

  • NG_023199.1:g.7560G>A
  • NM_002876.3:c.376G>A
  • NP_002867.1:p.Ala126Thr

Associated Genes

RAD51 Paralog C
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Genomic Location

chr17:58695161

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

61758784

Clinvar

132721

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.38LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B34' from family 11 in the publ...
114480.47LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B43' from family 20 in the publ...
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Contributors

  • Asha Deepthi: 22.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 22.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.