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ERBB2 c.1342C>A ;(p.L448M)
Variant ID: 17-37872021-C-A
NM_004448.2(
ERBB2
):c.1342C>A;(p.L448M)
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:
RTK-RAS pathway mutation is enriched in myeloid sarcoma.
Blood Cancer Journal
Choi, Mihong M; Jeon, Yoon Kyung YK; Sun, Choong-Hyun CH; Yun, Hong-Seok HS; Hong, Junshik J; Shin, Dong-Yeop DY; Kim, Inho I; Yoon, Sung-Soo SS; Koh, Youngil Y
Publication Date: 2018-05-23
Variant appearance in text: ERBB2: 1342C>A
PubMed Link:
29789584
Variant Present in the following documents:
Main text
41408_2018_Article_83.pdf
View BVdb publication page