NM_002176.4:c.498A>G

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  2. NM_002176.4:c.498A>G

HGVS Expressions

  • NM_002176.4:c.498A>G
  • NP_002167.1:p.Ile166Met
  • NC_000009.12:g.21077372T>C

Associated Genes

Interferon, Beta-1
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Clinvar Clinical Significance

Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

141894933

Clinvar

718451

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.41Lebanon1Uncertain SignificanceFamilial Mediterranean FeverUmar et al, 2020
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Contributors

  • Sayeeda Hana: 10.02.2021

Edit History

  • Sayeeda Hana: 17.02.2021
  • Sayeeda Hana: 11.02.2021
  • Sayeeda Hana: 10.02.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.