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KRAS c.450+2219T>C
Variant ID: 12-25376329-A-G
NM_004985.3(
KRAS
):c.450+2219T>C
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:
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: rs11047901
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.
Human Reproduction Update
Tempfer, C B CB; Simoni, M M; Destenaves, B B; Fauser, B C J M BC
Publication Date: 2009
Variant appearance in text: rs11047901
PubMed Link:
18805939
Variant Present in the following documents:
Main text
dmn040.pdf
View BVdb publication page