SLCO2B1 c.1596C>A ;(p.S532R)

Variant ID: 11-74907721-C-A

NM_007256.4(SLCO2B1):c.1596C>A;(p.S532R)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Exonic variants undergoing allele-specific selection in cancers.

Bmc Medical Genomics
Li, Qiyuan Q; Zeng, Yuanyuan Y; Wang, Janet J; Fang, Hongkun H; Guo, Jintao J; Yu, Liying L; Zhong, Taoling T; Xu, Chaoqun C; Freedman, Matthew M; LaFramboise, Thomas T
Publication Date: 2021-05-31

Variant appearance in text: rs61555831
PubMed Link: 34059054
Variant Present in the following documents:
  • Main text
  • 12920_2021_Article_984.pdf
View BVdb publication page



Decoding variants in drug-metabolizing enzymes and transporters in solid tumor patients by whole-exome sequencing.

Saudi Journal Of Biological Sciences
Aboul-Soud, Mourad A M MAM; Alzahrani, Alhussain J AJ; Mahmoud, Amer A
Publication Date: 2021-01

Variant appearance in text: rs61555831
PubMed Link: 33424349
Variant Present in the following documents:
  • mmc1.xlsx, sheet 1
View BVdb publication page



Targeted next generation sequencing as a tool for precision medicine.

Bmc Medical Genomics
Gulilat, Markus M; Lamb, Tyler T; Teft, Wendy A WA; Wang, Jian J; Dron, Jacqueline S JS; Robinson, John F JF; Tirona, Rommel G RG; Hegele, Robert A RA; Kim, Richard B RB; Schwarz, Ute I UI
Publication Date: 2019-06-03

Variant appearance in text: rs61555831
PubMed Link: 31159795
Variant Present in the following documents:
  • 12920_2019_527_MOESM1_ESM.xlsx, sheet 6
View BVdb publication page