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UGT1A3 c.1021_1022delinsTG ;(p.T341C)
Variant ID: 2-234676516-AC-TG
NM_019093.2(
UGT1A3
):c.1021_1022delinsTG;(p.T341C)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Crohn's disease in Japanese is associated with a SNP-haplotype of N-acetyltransferase 2 gene.
World Journal Of Gastroenterology
Machida, Haruhisa H; Tsukamoto, Kazuhiro K; Wen, Chun-Yang CY; Shikuwa, Saburou S; Isomoto, Hajime H; Mizuta, Yohei Y; Takeshima, Fuminao F; Murase, Kunihiko K; Matsumoto, Naomichi N; Murata, Ikuo I; Kohno, Shigeru S; Wen, Chen-Yang CY
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