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MED16 c.700_701delinsCC ;(p.S234P)
Variant ID: 19-885948-CT-GG
NM_005481.2(
MED16
):c.700_701delinsCC;(p.S234P)
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:
Cancer neoantigen prioritization through sensitive and reliable proteogenomics analysis.
Nature Communications
Wen, Bo B; Li, Kai K; Zhang, Yun Y; Zhang, Bing B
Publication Date: 2020-04-09
Variant appearance in text: MED16: S234P
PubMed Link:
32273506
Variant Present in the following documents:
41467_2020_15456_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page