NM_001142571.2:c.758A>G

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  2. NM_001142571.2:c.758A>G

HGVS Expressions

  • NG_031858.1:g.21576A>G
  • NM_001142571.2:c.758A>G
  • NP_001136043.1:p.Glu253Gly

Associated Genes

RAD51 Paralog D
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Genomic Location

chr17:35103294

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

28363284

Clinvar

138873

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.43LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B39' from family 16 in the publ...
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Contributors

  • Asha Deepthi: 13.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 13.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.