Variant ID: 20-43058096-C-G

NM_000457.4(HNF4A):c.1283-67C>G

This variant was identified in 2 publications




Publications:


Genetic variations of NR2A1 in Asian populations: implications in pharmacogenetics studies.

Drug Metabolism And Pharmacokinetics
SC Chew, JS Lim, EJ Lee, B Chowbay
Publication Date: 2013

Variant appearance in text: rs3746575
PubMed Link: 23268925
Variant Present in the following documents:
  • Supplemental file
  • Main text
View BVdb publication page



Association analysis of 33 lipoprotein candidate genes in multi-generational families of African ancestry.

Journal Of Lipid Research
I Miljkovic, LM Yerges-Armstrong, LH Kuller, AL Kuipers, X Wang, CM Kammerer, CS Nestlerode, CH Bunker, AL Patrick, VW Wheeler, RW Evans, JM Zmuda
Publication Date: 2010-07

Variant appearance in text: rs3746575
PubMed Link: 20308432
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000316099.4 c.1283-67C>G - intron_variant - 9/9
ENST00000316673.4 c.1217-67C>G - intron_variant - 9/9
ENST00000372920.1 c.*1050-67C>G - intron_variant,NMD_transcript_variant - 10/10
ENST00000415691.2 c.1253-67C>G - intron_variant - 9/9
ENST00000457232.1 c.1187-67C>G - intron_variant - 9/9
NM_000457.4 c.1283-67C>G - intron_variant - 9/9
NM_001030003.3 c.1187-67C>G - intron_variant - 9/9
NM_001258355.2 c.1262-67C>G - intron_variant - 10/10
NM_001287182.2 c.1178-67C>G - intron_variant - 10/10
NM_001287183.1 c.1208-67C>G - intron_variant - 10/10
NM_175914.4 c.1217-67C>G - intron_variant - 9/9
NM_178849.3 c.1253-67C>G - intron_variant - 9/9