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ERBB2 c.1898+86_1898+144del
Variant ID: 17-37873819-TCTCCCTTTGTCATATCTTGTTTCTGATGACAAAAATAACACATTGTTAAAATTGTAAAA-T
NM_004448.2(
ERBB2
):c.1898+86_1898+144del
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:
Clinical significance of ERBB2 exon 16 skipping: analysis of a real-world retrospective observational cohort study.
Esmo Open
Shi, Lei L; Xu, Caihua C; Ma, Yutong Y; Ou, Qiuxiang Q; Wu, Xue X; Lu, Songhua S; Shao, Yang Y; Guo, Renhua R; Kong, Jinliang J
Publication Date: 2020-11
Variant appearance in text: ERBB2: 1898+86_1946+50del
PubMed Link:
33214226
Variant Present in the following documents:
esmoopen-2020-000985supp001.pdf
View BVdb publication page