NM_002524.5:c.38G>A

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  2. NM_002524.5:c.38G>A

HGVS Expressions

  • NG_007572.1:g.5772G>A
  • NM_002524.5:c.38G>A
  • NP_002515.1:p.Gly13Asp
  • NC_000001.11:g.114716123C>T

Associated Genes

NRAS Protooncogene, GTPase
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Clinvar Clinical Significance

Likely Pathogenic, Pathogenic

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

dbSNP

121434596

Clinvar

13901

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
188550.G.1LebanonLikely PathogenicThyroid Carcinoma, PapillaryFakhruddin et al. 2017 253 cases of PTC
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Contributors

  • Pratibha Nair: 09.05.2021

Edit History

  • Pratibha Nair: 09.05.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.