NM_004629.2:c.1298G>C

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HGVS Expressions

  • NG_007887.1:g.2143G>C
  • NM_004629.2:c.1298G>C
  • NP_004620.1:p.Arg433Pro
  • NC_000009.12:g.35075600C>G

Associated Genes

FANCG Gene
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

748738986

Clinvar

836235

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.37LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B33' from family 10 in the publ...
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Contributors

  • Asha Deepthi: 22.09.2020

Edit History

  • Pratibha Nair: 09.11.2022
  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 22.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.