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RARA c.73_74delinsCT ;(p.A25L)
Variant ID: 17-38487543-GC-CT
NM_000964.3(
RARA
):c.73_74delinsCT;(p.A25L)
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:
Assessment of risk based on variant pathways and establishment of an artificial neural network model of thyroid cancer.
Bmc Medical Genetics
Zhao, Yinlong Y; Zhao, Lingzhi L; Mao, Tiezhu T; Zhong, Lili L
Publication Date: 2019-05-28
Variant appearance in text: RARA: A25L
PubMed Link:
31138213
Variant Present in the following documents:
12881_2019_829_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page