Bibliome.ai browser hg19
Search
About
Stats
FAQ
RUNX2 c.1529del ;(p.S510Mfs*69)
Variant ID: 6-45515005-AG-A
NM_001024630.3(
RUNX2
):c.1529del;(p.S510Mfs*69)
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:
Integrative pan cancer analysis reveals epigenomic variation in cancer type and cell specific chromatin domains.
Nature Communications
Gopi, Lijin K LK; Kidder, Benjamin L BL
Publication Date: 2021-03-03
Variant appearance in text: RUNX2: 1529delG
PubMed Link:
33658503
Variant Present in the following documents:
Main text
41467_2021_Article_21707.pdf
View BVdb publication page