SULT1A2 c.57G>A ;(p.P19=)

Variant ID: 16-28607195-C-T

NM_001054.3(SULT1A2):c.57G>A;(p.P19=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: SULT1A2: P19P
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2
View BVdb publication page



Relationship between genotypes Sult1a2 and Cyp2d6 and tamoxifen metabolism in breast cancer patients.

Plos One
Fernández-Santander, Ana A; Gaibar, María M; Novillo, Apolonia A; Romero-Lorca, Alicia A; Rubio, Margarita M; Chicharro, Luis Miguel LM; Tejerina, Armando A; Bandrés, Fernando F
Publication Date: 2013

Variant appearance in text: rs199986857
PubMed Link: 23922954
Variant Present in the following documents:
  • Main text
  • pone.0070183.pdf
View BVdb publication page