NM_000135.4:c.796A>G

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HGVS Expressions

  • NG_011706.1:g.22023A>G
  • NM_000135.4:c.796A>G
  • NP_000126.2:p.Thr266Ala

Associated Genes

FANCA Gene
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Genomic Location

chr16:89799635

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

7190823

Clinvar

134294

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.49LebanonAssociationBreast CancerJalkh et al, 2017 Patient 'B45' from family 22 in the publ...
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Contributors

  • Asha Deepthi: 09.09.2020

Edit History

  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 09.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.