NM_001199633.1:c.1381C>T

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HGVS Expressions

  • NM_001199633.1:c.1381C>T
  • NP_001186562.1:p.Leu461=
  • NC_000009.12:g.84286011G>A

Associated Genes

Solute Carrier Family 28 (Sodium-Coupled Nucleoside Transporter), Member 3
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Clinvar Clinical Significance

Benign

Variant Type

Substitution

dbSNP

7853758

Clinvar

375669

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
171050.G.1United Arab Emirates0.1111Al-Mahayri et al. 2020 100 (52 females, 48 males) normal health...
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Contributors

  • Pratibha Nair: 01.03.2022

Edit History

  • Sayeeda Hana: 13.01.2023
  • Pratibha Nair: 01.03.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.