PAH c.1006C>T ;(p.Q336*)

Variant ID: 12-103238173-G-A

NM_000277.1(PAH):c.1006C>T;(p.Q336*)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Application of a next-generation sequencing (NGS) panel in newborn screening efficiently identifies inborn disorders of neonates.

Orphanet Journal Of Rare Diseases
Huang, Xinwen X; Wu, Dingwen D; Zhu, Lin L; Wang, Wenjun W; Yang, Rulai R; Yang, Jianbin J; He, Qunyan Q; Zhu, Bingquan B; You, Ying Y; Xiao, Rui R; Zhao, Zhengyan Z
Publication Date: 2022-02-21

Variant appearance in text: PAH: 1006C>T
PubMed Link: 35193651
Variant Present in the following documents:
  • 13023_2022_2231_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Hou, Ying-Chen Claire YC; Yu, Hung-Chun HC; Martin, Rick R; Cirulli, Elizabeth T ET; Schenker-Ahmed, Natalie M NM; Hicks, Michael M; Cohen, Isaac V IV; Jönsson, Thomas J TJ; Heister, Robyn R; Napier, Lori L; Swisher, Christine Leon CL; Dominguez, Saints S; Tang, Haibao H; Li, Weizhong W; Perkins, Bradley A BA; Barea, Jaime J; Rybak, Christina C; Smith, Emily E; Duchicela, Keegan K; Doney, Michael M; Brar, Pamila P; Hernandez, Nathaniel N; Kirkness, Ewen F EF; Kahn, Andrew M AM; Venter, J Craig JC; Karow, David S DS; Caskey, C Thomas CT
Publication Date: 2020-02-11

Variant appearance in text: PAH: 1006C>T
PubMed Link: 31980526
Variant Present in the following documents:
  • pnas.1909378117.sapp.pdf
View BVdb publication page



Mutation spectrum of six genes in Chinese phenylketonuria patients obtained through next-generation sequencing.

Plos One
Gu, Ying Y; Lu, Kangmo K; Yang, Guanghui G; Cen, Zhong Z; Yu, Li L; Lin, Lin L; Hao, Jing J; Yang, Zhigang Z; Peng, Jiabao J; Cui, Shujian S; Huang, Jian J
Publication Date: 2014

Variant appearance in text: PAH: 1006C>T; Q336X
PubMed Link: 24705691
Variant Present in the following documents:
  • Main text
  • pone.0094100.pdf
  • pone.0094100.s010.xlsx, sheet 1
  • pone.0094100.s009.xlsx, sheet 1
View BVdb publication page



Investigation of parameters that affect the success rate of microarray-based allele-specific hybridization assays.

Plos One
Poulsen, Lena L; Søe, Martin Jensen MJ; Møller, Lisbeth Birk LB; Dufva, Martin M
Publication Date: 2011-03-22

Variant appearance in text: PAH: 1006C>T; Q336X
PubMed Link: 21445337
Variant Present in the following documents:
  • Main text
  • pone.0014777.pdf
View BVdb publication page