PTPN22 c.77A>G ;(p.N26S)

Variant ID: 1-114414169-T-C

NM_015967.5(PTPN22):c.77A>G;(p.N26S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic Polymorphism of PTPN22 in Autoimmune Diseases: A Comprehensive Review.

Medicina (Kaunas, Lithuania)
Tizaoui, Kalthoum K; Shin, Jae Il JI; Jeong, Gwang Hun GH; Yang, Jae Won JW; Park, Seoyeon S; Kim, Ji Hong JH; Hwang, Soo Young SY; Park, Se Jin SJ; Koyanagi, Ai A; Smith, Lee L
Publication Date: 2022-08-02

Variant appearance in text: PTPN22: 77A>G
PubMed Link: 36013501
Variant Present in the following documents:
  • Main text
  • medicina-58-01034.pdf
View BVdb publication page



Novel missense mutation in PTPN22 in a Chinese pedigree with Hashimoto's thyroiditis.

Bmc Endocrine Disorders
Gong, Licheng L; Liu, Beihong B; Wang, Jing J; Pan, Hong H; Qi, Anhui A; Zhang, Siyang S; Wu, Jinyi J; Yang, Ping P; Wang, Binbin B
Publication Date: 2018-11-01

Variant appearance in text: PTPN22: Asn26Ser
PubMed Link: 30384852
Variant Present in the following documents:
  • Main text
  • 12902_2018_Article_305.pdf
View BVdb publication page