NM_022725.4:c.959C>T

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HGVS Expressions

  • NG_007425.1:g.5990C>T
  • NM_022725.4:c.959C>T
  • NP_073562.1:p.Pro320Leu

Associated Genes

FANCF Gene
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Genomic Location

chr11:22624852

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

45451294

Clinvar

134351

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.