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DNAH11 c.1072_1074delinsTGG ;(p.R358W)
Variant ID: 7-21603893-CGC-TGG
NM_001277115.1(
DNAH11
):c.1072_1074delinsTGG;(p.R358W)
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:
Identification and ranking of recurrent neo-epitopes in cancer.
Bmc Medical Genomics
Blanc, Eric E; Holtgrewe, Manuel M; Dhamodaran, Arunraj A; Messerschmidt, Clemens C; Willimsky, Gerald G; Blankenstein, Thomas T; Beule, Dieter D
Publication Date: 2019-11-27
Variant appearance in text: DNAH11: R358W
PubMed Link:
31775766
Variant Present in the following documents:
12920_2019_611_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page