Bibliome.ai browser hg19
Search
About
Stats
FAQ
EGR1 c.1135_1136insA ;(p.R379Qfs*32)
Variant ID: 5-137803273-C-CA
NM_001964.2(
EGR1
):c.1135_1136insA;(p.R379Qfs*32)
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:
Human BRCA pathogenic variants were originated during recent human history.
Life Science Alliance
Li, Jiaheng J; Zhao, Bojin B; Huang, Teng T; Qin, Zixin Z; Wang, San Ming SM
Publication Date: 2022-05
Variant appearance in text: 225: 1135_1136insA
PubMed Link:
35165121
Variant Present in the following documents:
Main text
LSA-2021-01263.pdf
View BVdb publication page