NM_033360.4:c.34G>T

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HGVS Expressions

  • NG_007524.1:g.10570G>T
  • NM_033360.4:c.34G>T
  • NP_203524.1:p.Gly12Cys

Associated Genes

KRAS Proto-Oncogene, GTPase
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Genomic Location

chr12:25245351

Clinvar Clinical Significance

Likely Pathogenic, Pathogenic

CTGA Clinical Significance

Likely Pathogenic, Pathogenic

Variant Type

Substitution

dbSNP

121913530

Clinvar

12578

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
211980.G.4.1LebanonLikely Pathogenic, PathogenicLung CancerFakhruddin et al, 2014 19 patients from a study that included 1...
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Contributors

  • Asha Deepthi: 01.07.2020

Edit History

  • Asha Deepthi: 02.07.2020
  • Asha Deepthi: 01.07.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.