NM_000135.4:c.4249C>G

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HGVS Expressions

  • NG_011706.1:g.82765C>G
  • NM_000135.4:c.4249C>G
  • NP_000126.2:p.His1417Tyr

Associated Genes

FANCA Gene
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Genomic Location

chr16:89738893

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

17227403

Clinvar

134282

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
227650.5Lebanon2Likely BenignFanconi Anemia, Complementation Group AFarah et al. 2020
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Contributors

  • Pratibha Nair: 21.09.2020

Edit History

  • Pratibha Nair: 21.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.