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RARA c.179-327A>G
Variant ID: 17-38504241-A-G
NM_000964.3(
RARA
):c.179-327A>G
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.
Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11
Variant appearance in text: rs482284
PubMed Link:
36467812
Variant Present in the following documents:
JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page
Pathway-Targeted Pharmacogenomics of CYP1A2 in Human Liver.
Frontiers In Pharmacology
Klein, Kathrin K; Winter, Stefan S; Turpeinen, Miia M; Schwab, Matthias M; Zanger, Ulrich M UM
Publication Date: 2010
Variant appearance in text: rs482284
PubMed Link:
21918647
Variant Present in the following documents:
Main text
fphar-01-00129.pdf
View BVdb publication page
The retinoic acid receptor alpha (RARA) gene is not associated with myopia, hypermetropia, and ocular biometric measures.
Molecular Vision
Veerappan, S S; Schäche, M M; Pertile, K K KK; Islam, F M A FM; Chen, C Y CY; Mitchell, P P; Dirani, M M; Baird, P N PN
Publication Date: 2009-07-17
Variant appearance in text: rs482284
PubMed Link:
19626135
Variant Present in the following documents:
Main text
mv-v15-1390.pdf
View BVdb publication page