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LAMP3 c.888+345C>T
Variant ID: 3-182869818-G-A
NM_014398.3(
LAMP3
):c.888+345C>T
This variant was identified in 7 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: rs683395
PubMed Link:
36467812
Variant Present in the following documents:
JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page
Replicability analysis in genome-wide association studies via Cartesian hidden Markov models.
Bmc Bioinformatics
Wang, Pengfei P; Zhu, Wensheng W
Publication Date: 2019-03-18
Variant appearance in text: rs683395
PubMed Link:
30885122
Variant Present in the following documents:
Main text
12859_2019_Article_2707.pdf
View BVdb publication page
Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.
Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018
Variant appearance in text: LAMP3: 888+345C>T; rs683395
PubMed Link:
30319441
Variant Present in the following documents:
Table_7.xlsx, sheet 1
Table_6.xlsx, sheet 1
View BVdb publication page
Genetic Variants Involved in Bipolar Disorder, a Rough Road Ahead.
Clinical Practice And Epidemiology In Mental Health : Cp & Emh
Orrù, Germano G; Carta, Mauro Giovanni MG
Publication Date: 2018
Variant appearance in text: rs683395
PubMed Link:
29541150
Variant Present in the following documents:
CPEMH-14-37.pdf
View BVdb publication page
Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
Genetic Epidemiology
Jiang, Yuan Y; Zhang, Heping H
Publication Date: 2011-02
Variant appearance in text: rs683395
PubMed Link:
21254220
Variant Present in the following documents:
Main text
View BVdb publication page
Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort.
Molecular Psychiatry
Ollila, H M HM; Soronen, P P; Silander, K K; Palo, O M OM; Kieseppä, T T; Kaunisto, M A MA; Lönnqvist, J J; Peltonen, L L; Partonen, T T; Paunio, T T
Publication Date: 2009-04
Variant appearance in text: rs683395
PubMed Link:
19308021
Variant Present in the following documents:
Main text
View BVdb publication page
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
Nature
,
Publication Date: 2007-06-07
Variant appearance in text: rs683395
PubMed Link:
17554300
Variant Present in the following documents:
Main text
View BVdb publication page