NM_033360.4:c.38G>A

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  2. NM_033360.4:c.38G>A

HGVS Expressions

  • NG_007524.1:g.10574G>A
  • NM_033360.4:c.38G>A
  • NP_203524.1:p.Gly13Asp

Associated Genes

KRAS Proto-Oncogene, GTPase
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Genomic Location

chr12:25245347

Clinvar Clinical Significance

Likely Pathogenic, Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

dbSNP

112445441

Clinvar

12580

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
211980.G.4.6LebanonPathogenicLung CancerFakhruddin et al, 2014 Two patients from a study that included ...
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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.