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ATM c.5918+37T>C
Variant ID: 11-108181079-T-C
NM_000051.3(
ATM
):c.5918+37T>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:
Genetic heterogeneity in hepatocellular carcinoma and paired bone metastasis revealed by next-generation sequencing.
International Journal Of Clinical And Experimental Pathology
Jin, Ketao K; Lan, Huanrong H; Wang, Xuanwei X; Lv, Jieqing J
Publication Date: 2017
Variant appearance in text: ATM: 5918+37T>C
PubMed Link:
31966388
Variant Present in the following documents:
Main text
View BVdb publication page