ASAH1 c.383-374T>C

Variant ID: 8-17922414-A-G

NM_177924.3(ASAH1):c.383-374T>C

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Advanced bioinformatic analysis and pathway prediction of NSCLC cells upon cisplatin resistance.

Scientific Reports
Hossian, A K M Nawshad AKMN; Zahra, Fatema Tuz FT; Poudel, Sagun S; Abshire, Camille F CF; Polk, Paula P; Garai, Jone J; Zabaleta, Jovanny J; Mikelis, Constantinos M CM; Mattheolabakis, George G
Publication Date: 2021-03-22

Variant appearance in text: ASAH1: 382+2315T>C
PubMed Link: 33753779
Variant Present in the following documents:
  • 41598_2021_85930_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page



Acid ceramidase deficiency: Farber disease and SMA-PME.

Orphanet Journal Of Rare Diseases
Yu, Fabian P S FPS; Amintas, Samuel S; Levade, Thierry T; Medin, Jeffrey A JA
Publication Date: 2018-07-20

Variant appearance in text: rs7830490
PubMed Link: 30029679
Variant Present in the following documents:
  • Main text
  • 13023_2018_Article_845.pdf
View BVdb publication page



Research in China on the molecular genetics of schizophrenia.

Shanghai Archives Of Psychiatry
Cui, Donghong D; Jiang, Kaida K
Publication Date: 2012-08

Variant appearance in text: rs7830490
PubMed Link: 25324626
Variant Present in the following documents:
  • Main text
  • sap-24-04-187.pdf
View BVdb publication page



Kernel machine SNP-set analysis for censored survival outcomes in genome-wide association studies.

Genetic Epidemiology
Lin, Xinyi X; Cai, Tianxi T; Wu, Michael C MC; Zhou, Qian Q; Liu, Geoffrey G; Christiani, David C DC; Lin, Xihong X
Publication Date: 2011-11

Variant appearance in text: rs7830490
PubMed Link: 21818772
Variant Present in the following documents:
  • Main text
View BVdb publication page