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EGFR c.1536C>G ;(p.P512=)
Variant ID: 7-55229229-C-G
NM_005228.3(
EGFR
):c.1536C>G;(p.P512=)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genetic variants of the EGFR ligand-binding domain and their association with structural alterations in Arab cancer patients.
Bmc Research Notes
Marzouq, Maryam M; Nairouz, Ali A; Ben Khalaf, Noureddine N; Bourguiba-Hachemi, Sonia S; Quaddorah, Raed R; Ashoor, Dana D; Fathallah, M Dahmani MD
Publication Date: 2021-04-19
Variant appearance in text: N/A
PubMed Link:
33874989
Variant Present in the following documents:
View BVdb publication page
Circulating tumour DNA sequence analysis as an alternative to multiple myeloma bone marrow aspirates.
Nature Communications
Kis, Olena O; Kaedbey, Rayan R; Chow, Signy S; Danesh, Arnavaz A; Dowar, Mark M; Li, Tiantian T; Li, Zhihua Z; Liu, Jessica J; Mansour, Mark M; Masih-Khan, Esther E; Zhang, Tong T; Bratman, Scott V SV; Oza, Amit M AM; Kamel-Reid, Suzanne S; Trudel, Suzanne S; Pugh, Trevor J TJ
Publication Date: 2017-05-11
Variant appearance in text: N/A
PubMed Link:
28492226
Variant Present in the following documents:
View BVdb publication page