NM_005236.3:c.1633G>C

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HGVS Expressions

  • NG_011442.1:g.20409G>C
  • NM_005236.3:c.1633G>C
  • NP_005227.1:p.Gly545Arg

Associated Genes

Excision-Repair, Complementing Defective, In Chinese Hamster, 4
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Genomic Location

chr16:13935565

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

773007457

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.51LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B47' from family 37 in the publ...
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Contributors

  • Asha Deepthi: 29.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 29.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.