Variant ID: 2-234676516-AC-TG

NM_019093.2(UGT1A3):c.1021_1022delinsTG;(p.Thr341Cys)

This variant was identified in 1 publication




Publications:


Crohn's disease in Japanese is associated with a SNP-haplotype of N-acetyltransferase 2 gene.

World Journal Of Gastroenterology
H Machida, K Tsukamoto, CY Wen, S Shikuwa, H Isomoto, Y Mizuta, F Takeshima, K Murase, N Matsumoto, I Murata, S Kohno, CY Wen
Publication Date: 2005-08-21

Variant appearance in text: UGT1A3: T341C
PubMed Link: 16097053
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000305139.6 c.1015_1016delinsTG p.Thr339Cys missense_variant 3/5 -
ENST00000305208.5 c.1018_1019delinsTG p.Thr340Cys missense_variant 3/5 -
ENST00000344644.5 c.1009_1010delinsTG p.Thr337Cys missense_variant 3/5 -
ENST00000354728.4 c.1009_1010delinsTG p.Thr337Cys missense_variant 3/5 -
ENST00000360418.3 c.1018_1019delinsTG p.Thr340Cys missense_variant 3/5 -
ENST00000373409.3 c.1021_1022delinsTG p.Thr341Cys missense_variant 3/5 -
ENST00000373414.3 c.1021_1022delinsTG p.Thr341Cys missense_variant 3/5 -
ENST00000373424.1 c.214_215delinsTG p.Thr72Cys missense_variant 4/6 -
ENST00000373426.3 c.1009_1010delinsTG p.Thr337Cys missense_variant 3/5 -
ENST00000373445.1 c.1009_1010delinsTG p.Thr337Cys missense_variant 3/5 -
ENST00000373450.4 c.1009_1010delinsTG p.Thr337Cys missense_variant 3/5 -
ENST00000406651.1 c.214_215delinsTG p.Thr72Cys missense_variant 3/5 -
ENST00000446481.2 c.214_215delinsTG p.Thr72Cys missense_variant,NMD_transcript_variant 4/7 -
ENST00000450233.1 c.1021_1022delinsTG p.Thr341Cys missense_variant,NMD_transcript_variant 3/6 -
ENST00000482026.1 c.1021_1022delinsTG p.Thr341Cys missense_variant 3/5 -
ENST00000608381.1 c.1021_1022delinsTG p.Thr341Cys missense_variant 3/5 -
ENST00000608383.1 c.1018_1019delinsTG p.Thr340Cys missense_variant 3/5 -
ENST00000609637.1 c.1009_1010delinsTG p.Thr337Cys missense_variant 3/5 -
ENST00000609767.1 c.1021_1022delinsTG p.Thr341Cys missense_variant 3/5 -
NM_000463.3 c.1018_1019delinsTG p.Thr340Cys missense_variant 3/5 -
NM_001072.4 c.1015_1016delinsTG p.Thr339Cys missense_variant 3/5 -
NM_007120.3 c.1021_1022delinsTG p.Thr341Cys missense_variant 3/5 -
NM_019075.2 c.1009_1010delinsTG p.Thr337Cys missense_variant 3/5 -
NM_019076.4 c.1009_1010delinsTG p.Thr337Cys missense_variant 3/5 -
NM_019077.2 c.1009_1010delinsTG p.Thr337Cys missense_variant 3/5 -
NM_019078.1 c.1021_1022delinsTG p.Thr341Cys missense_variant 3/5 -
NM_019093.2 c.1021_1022delinsTG p.Thr341Cys missense_variant 3/5 -
NM_021027.3 c.1009_1010delinsTG p.Thr337Cys missense_variant 3/5 -
NM_205862.2 c.214_215delinsTG p.Thr72Cys missense_variant 4/6 -