Variant ID: 2-113590389-C-T

NM_000576.2(IL1B):c.316G>A;(p.Asp106Asn)

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: rs139843362
PubMed Link: 24754437
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000263341.2 c.316G>A p.Asp106Asn missense_variant 5/7 -
ENST00000416750.1 c.316G>A p.Asp106Asn missense_variant 5/5 -
ENST00000418817.1 c.316G>A p.Asp106Asn missense_variant 5/5 -
ENST00000432018.1 c.316G>A p.Asp106Asn missense_variant 4/4 -
ENST00000487639.1 n.217G>A - non_coding_transcript_exon_variant 2/3 -
ENST00000491056.1 n.1123G>A - non_coding_transcript_exon_variant 4/6 -
NM_000576.3 c.316G>A p.Asp106Asn missense_variant 5/7 -