NM_006297.3:c.580C>T

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HGVS Expressions

  • NG_033799.1:g.27157C>T
  • NM_006297.3:c.580C>T
  • NP_006288.2:p.Arg194Trp

Associated Genes

X-Ray Repair, Complementing Defective, in Chinese Hamster, 1
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Genomic Location

chr19:43553422

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

1799782

Clinvar

376355

Epidemiology in the Arab World

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

  • Asha Deepthi: 06.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 30.09.2020
  • Asha Deepthi: 06.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.