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RET c.2172G>C ;(p.L724F)
Variant ID: 10-43612067-G-C
NM_020975.4(
RET
):c.2172G>C;(p.L724F)
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:
Identification of RUNX1T1 as a potential epigenetic modifier in small-cell lung cancer.
Molecular Oncology
He, Tian T; Wildey, Gary G; McColl, Karen K; Savadelis, Alyssa A; Spainhower, Kyle K; McColl, Cassidy C; Kresak, Adam A; Tan, Aik Choon AC; Yang, Michael M; Abbas, Ata A; Dowlati, Afshin A
Publication Date: 2021-01
Variant appearance in text: RET: L724F
PubMed Link:
33084222
Variant Present in the following documents:
Main text
MOL2-15-195.pdf
View BVdb publication page
Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.
Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09
Variant appearance in text: RET: L724F
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page