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KRAS c.-12+329G>A
Variant ID: 12-25403356-C-T
NM_004985.5(
KRAS
):c.-12+329G>A
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Association Study of Genetic Variants in Autophagy Pathway and Risk of Non-syndromic Cleft Lip With or Without Cleft Palate.
Frontiers In Cell And Developmental Biology
Lou, Shu S; Ma, Lan L; Kan, Shiyi S; Yu, Xin X; Wang, Yuting Y; Yang, Fan F; Zhu, Guirong G; Fan, Liwen L; Li, Dandan D; Wang, Hua H; Wang, Wei W; Zhang, Weibing W; Wang, Lin L; Pan, Yongchu Y
Publication Date: 2020
Variant appearance in text: rs147920828
PubMed Link:
32766242
Variant Present in the following documents:
Main text
fcell-08-00576.pdf
View BVdb publication page
Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.
The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04
Variant appearance in text: rs147920828
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page