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EPN3 c.*999G>T
Variant ID: 17-48620517-G-T
NM_017957.2(
EPN3
):c.*999G>T
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:
Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.
Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10
Variant appearance in text: rs4793661
PubMed Link:
29221171
Variant Present in the following documents:
oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page
High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene.
Molecular Psychiatry
Strom, S P SP; Stone, J L JL; Ten Bosch, J R JR; Merriman, B B; Cantor, R M RM; Geschwind, D H DH; Nelson, S F SF
Publication Date: 2010-10
Variant appearance in text: rs4793661
PubMed Link:
19455149
Variant Present in the following documents:
Main text
View BVdb publication page