NM_005514.7:c.97T>C

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  2. NM_005514.7:c.97T>C

HGVS Expressions

  • NG_023187.1:g.5279T>C
  • NM_005514.7:c.97T>C
  • NP_005505.2:p.Tyr33His
  • NC_000006.12:g.31356934A>G

Associated Genes

Major Histocompatibility Complex, Class I, B
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CTGA Clinical Significance

Risk factor

Variant Type

Substitution

dbSNP

2596492

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
109650.G.5Saudi ArabiaRisk factorBehçet SyndromeAndo et al. 1997 Family with unknown number of members ca...
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Contributors

  • Sayeeda Hana: 25.12.2019

Edit History

  • Precise Support: 08.11.2022
  • Sami Bizzari: 12.09.2022
  • Rahila Mir: 22.02.2022
  • Sami Bizzari: 07.05.2020
  • Sayeeda Hana: 25.12.2019
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.