NM_017852.4:c.2672G>T

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  2. NM_017852.4:c.2672G>T

HGVS Expressions

  • NG_052633.1:g.42507G>T
  • NM_017852.4:c.2672G>T
  • NP_060322.1:p.Gly891Val
  • NC_000019.10:g.54990636G>T

Associated Genes

NLR Family, Pyrin Domain-Containing 2
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

2072412386

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.30Lebanon1Uncertain SignificanceFamilial Mediterranean FeverUmar et al, 2020
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Contributors

  • Sayeeda Hana: 12.02.2021

Edit History

  • Rahila Mir: 22.02.2022
  • Sayeeda Hana: 22.09.2021
  • Sayeeda Hana: 16.02.2021
  • Sayeeda Hana: 12.02.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.