Variant ID: 1-183668577-T-A

NM_015149.3(RGL1):c.-32-42684T>A

This variant was identified in 1 publication




Publications:


IL-1β associations with posttraumatic epilepsy development: a genetics and biomarker cohort study.

Epilepsia
ML Diamond, AC Ritter, MD Failla, JA Boles, YP Conley, PM Kochanek, AK Wagner
Publication Date: 2014-07

Variant appearance in text: rs114640380
PubMed Link: 24754437
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000304685.4 c.-32-42684T>A - intron_variant - 1/18
ENST00000536277.1 c.-33+1930T>A - intron_variant - 2/18
NM_001297669.2 c.-33+1930T>A - intron_variant - 2/18
NM_001297670.2 c.-32-42684T>A - intron_variant - 1/17
NM_015149.5 c.-32-42684T>A - intron_variant - 1/18