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HR c.1705_1706delinsTC ;(p.L569S)
Variant ID: 8-21982868-AG-GA
NM_005144.4(
HR
):c.1705_1706delinsTC;(p.L569S)
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:
Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.
Scientific Reports
Fransson, Susanne S; Martinez-Monleon, Angela A; Johansson, Mathias M; Sjöberg, Rose-Marie RM; Björklund, Caroline C; Ljungman, Gustaf G; Ek, Torben T; Kogner, Per P; Martinsson, Tommy T
Publication Date: 2020-12-31
Variant appearance in text: HR: L569S
PubMed Link:
33384420
Variant Present in the following documents:
Main text
View BVdb publication page