NM_000882.4:c.631G>A

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  2. NM_000882.4:c.631G>A

HGVS Expressions

  • NG_033022.1:g.11593G>A
  • NM_000882.4:c.631G>A
  • NP_000873.2:p.Val211Met
  • NC_000003.12:g.159995428G>A

Associated Genes

Interleukin 12A
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Clinvar Clinical Significance

Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

35990253

Clinvar

708885

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.16Lebanon1Uncertain SignificanceUmar et al, 2020
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Contributors

  • Sayeeda Hana: 11.02.2021

Edit History

  • Sayeeda Hana: 15.02.2021
  • Sayeeda Hana: 11.02.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.