NM_033084.6:c.1348A>G

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HGVS Expressions

  • NG_007311.1:g.26558A>G
  • NM_033084.6:c.1348A>G
  • NP_149075.2:p.Ile450Val

Associated Genes

FANCD2 Gene
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Genomic Location

chr3:10047986

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

145129959

Clinvar

456344

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.52LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B48' from family 38 in the publ...
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Contributors

  • Asha Deepthi: 28.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 28.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.