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CP c.1348+9T>C
Variant ID: 3-148919880-A-G
NM_000096.3(
CP
):c.1348+9T>C
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:
Systematic Review of Genetic Factors in the Etiology of Esophageal Squamous Cell Carcinoma in African Populations.
Frontiers In Genetics
Simba, Hannah H; Kuivaniemi, Helena H; Lutje, Vittoria V; Tromp, Gerard G; Sewram, Vikash V
Publication Date: 2019
Variant appearance in text: rs35272481
PubMed Link:
31428123
Variant Present in the following documents:
Main text
fgene-10-00642.pdf
View BVdb publication page