NM_002661.5:c.82A>T

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  2. NM_002661.5:c.82A>T

HGVS Expressions

  • NG_032019.2:g.51975A>T
  • NM_002661.5:c.82A>T
  • NP_002652.2:p.Met28Leu
  • NC_000016.10:g.81786071A>T

Associated Genes

Phospholipase C, Gamma-2
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

61749044

Clinvar

440153

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.13Lebanon1Uncertain SignificanceUmar et al, 2020
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Contributors

  • Sayeeda Hana: 07.02.2021

Edit History

  • Sayeeda Hana: 15.02.2021
  • Sayeeda Hana: 14.02.2021
  • Sayeeda Hana: 07.02.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.