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ALG9 c.1733+1105G>A
Variant ID: 11-111679262-C-T
NM_024740.2(
ALG9
):c.1733+1105G>A
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:
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: rs4935811
PubMed Link:
36467812
Variant Present in the following documents:
JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page
Common variations in ALG9 are not associated with bipolar I disorder: a family-based study.
Behavioral And Brain Functions : Bbf
Baysal, Bora E BE; Willett-Brozick, Joan E JE; Bacanu, Silviu-Alin SA; Detera-Wadleigh, Sevilla S; Nimgaonkar, Vishwajit L VL
Publication Date: 2006-07-21
Variant appearance in text: rs4935811
PubMed Link:
16859551
Variant Present in the following documents:
1744-9081-2-25-S1.xls, sheet 1
View BVdb publication page