NM_002693.3:c.2734+39_2734+40insAGGT

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HGVS Expressions

  • NG_008218.2:g.18710_18711insGTAG
  • NM_002693.3:c.2734+39_2734+40insAGGT
  • NP_002684.1:p.?
  • NC_000015.10:g.89321085_89321086insACCT

Associated Genes

Polymerase, DNA, Gamma
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Clinvar Clinical Significance

Benign

Variant Type

Insertion

dbSNP

2307433

Clinvar

619386

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605977.G.1United Arab Emirates0.514Almheiri et al. 2019 500 healthy Emiratis (254 females)
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Contributors

  • Pratibha Nair: 17.03.2022

Edit History

  • Pratibha Nair: 06.12.2022
  • Pratibha Nair: 22.03.2022
  • Pratibha Nair: 17.03.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.