NM_005432.4:c.260C>T

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  2. NM_005432.4:c.260C>T

HGVS Expressions

  • NG_011516.1:g.13338C>T
  • NM_005432.4:c.260C>T
  • NP_005423.1:p.Pro87Leu

Associated Genes

X-Ray Repair, Complementing Defective, in Chinese Hamster, 3
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Genomic Location

chr14:103707149

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

749386482

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.53LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B49' from family 24 in the publ...
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Contributors

  • Asha Deepthi: 06.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 06.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.