Bibliome.ai browser hg19
Search
About
Stats
FAQ
RYR1 c.11135A>G ;(p.E3712G)
Variant ID: 19-39019691-A-G
NM_000540.2(
RYR1
):c.11135A>G;(p.E3712G)
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:
Mutational landscape and potential therapeutic targets for sporadic pancreatic neuroendocrine tumors based on target next-generation sequencing.
Experimental And Therapeutic Medicine
Zheng, Kailian K; Liu, Tao T; Zhao, Jiangman J; Meng, Peng P; Bian, Yun Y; Ni, Chenming C; Wang, Huan H; Pan, Yaqi Y; Wu, Shouxin S; Jiang, Hui H; Jin, Gang G
Publication Date: 2021-05
Variant appearance in text: RYR1: E3712G
PubMed Link:
33747156
Variant Present in the following documents:
Supplementary_Data3.xlsx, sheet 1
View BVdb publication page