SLCO1B1 c.1198T>G ;(p.F400V)

Variant ID: 12-21355487-T-G

NM_006446.4(SLCO1B1):c.1198T>G;(p.F400V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical pharmacogenetic analysis in 5,001 individuals with diagnostic Exome Sequencing data.

Npj Genomic Medicine
Lanillos, Javier J; Carcajona, Marta M; Maietta, Paolo P; Alvarez, Sara S; Rodriguez-Antona, Cristina C
Publication Date: 2022-02-18

Variant appearance in text: SLCO1B1: F400V
PubMed Link: 35181665
Variant Present in the following documents:
  • 41525_2022_283_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page