NM_006297.3:c.839G>A

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HGVS Expressions

  • NG_033799.1:g.28319G>A
  • NM_006297.3:c.839G>A
  • NP_006288.2:p.Arg280His

Associated Genes

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

chr19:43552260

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

25489

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.26LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B19' from family 1 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.