NM_001354609.1:c.1799T>A

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  2. NM_001354609.1:c.1799T>A

HGVS Expressions

  • NG_007873.3:g.176429T>A
  • NM_001354609.1:c.1799T>A
  • NP_001341538.1:p.Val600Glu
  • NC_000007.14:g.140753336A>T

Associated Genes

B-Raf Protooncogene, Serine/Threonine Kinase
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Clinvar Clinical Significance

Drug Response, Likely Pathogenic, Pathogenic

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

dbSNP

113488022

Clinvar

376288

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.