APOA1 c.138C>T ;(p.L46=)

Variant ID: 11-116707779-G-A

NM_000039.1(APOA1):c.138C>T;(p.L46=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Targeted next-generation sequencing to diagnose disorders of HDL cholesterol.

Journal Of Lipid Research
Sadananda, Singh N SN; Foo, Jia Nee JN; Toh, Meng Tiak MT; Cermakova, Lubomira L; Trigueros-Motos, Laia L; Chan, Teddy T; Liany, Herty H; Collins, Jennifer A JA; Gerami, Sima S; Singaraja, Roshni R RR; Hayden, Michael R MR; Francis, Gordon A GA; Frohlich, Jiri J; Khor, Chiea Chuen CC; Brunham, Liam R LR
Publication Date: 2015-10

Variant appearance in text: APOA1: 138C>T
PubMed Link: 26255038
Variant Present in the following documents:
  • Main text
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