Bibliome.ai browser hg19
Search
About
Stats
FAQ
FAM86B2 c.10G>A ;(p.E4K)
Variant ID: 8-12293843-C-T
NM_001137610.1(
FAM86B2
):c.10G>A;(p.E4K)
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:
The landscape of driver mutations in cutaneous squamous cell carcinoma.
Npj Genomic Medicine
Chang, Darwin D; Shain, A Hunter AH
Publication Date: 2021-07-16
Variant appearance in text: FAM86B2: E4K
PubMed Link:
34272401
Variant Present in the following documents:
41525_2021_226_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page