CD22 c.2234G>C ;(p.G745A)

Variant ID: 19-35836530-G-C

NM_001771.3(CD22):c.2234G>C;(p.G745A)

This variant was identified in 12 publications

View GRCh38 version.




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: rs10406069
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



MicroRNAs and the Diagnosis of Childhood Acute Lymphoblastic Leukemia: Systematic Review, Meta-Analysis and Re-Analysis with Novel Small RNA-Seq Tools.

Cancers
Kyriakidis, Ioannis I; Kyriakidis, Konstantinos K; Tsezou, Aspasia A
Publication Date: 2022-08-17

Variant appearance in text: rs10406069
PubMed Link: 36010971
Variant Present in the following documents:
  • cancers-14-03976.pdf
View BVdb publication page



Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions.

Npj Parkinson'S Disease
Cukier, Holly N HN; Kim, Hyunjin H; Griswold, Anthony J AJ; Codreanu, Simona G SG; Prince, Lisa M LM; Sherrod, Stacy D SD; McLean, John A JA; Dykxhoorn, Derek M DM; Ess, Kevin C KC; Hedera, Peter P; Bowman, Aaron B AB; Neely, M Diana MD
Publication Date: 2022-06-29

Variant appearance in text: rs10406069
PubMed Link: 35768426
Variant Present in the following documents:
  • 41531_2022_346_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Implication of microRNAs in Carcinogenesis with Emphasis on Hematological Malignancies and Clinical Translation.

International Journal Of Molecular Sciences
Gaál, Zsuzsanna Z
Publication Date: 2022-05-23

Variant appearance in text: rs10406069
PubMed Link: 35628648
Variant Present in the following documents:
  • Main text
  • ijms-23-05838.pdf
View BVdb publication page



A reference collection of patient-derived cell line and xenograft models of proneural, classical and mesenchymal glioblastoma.

Scientific Reports
Stringer, Brett W BW; Day, Bryan W BW; D'Souza, Rochelle C J RCJ; Jamieson, Paul R PR; Ensbey, Kathleen S KS; Bruce, Zara C ZC; Lim, Yi Chieh YC; Goasdoué, Kate K; Offenhäuser, Carolin C; Akgül, Seçkin S; Allan, Suzanne S; Robertson, Thomas T; Lucas, Peter P; Tollesson, Gert G; Campbell, Scott S; Winter, Craig C; Do, Hongdo H; Dobrovic, Alexander A; Inglis, Po-Ling PL; Jeffree, Rosalind L RL; Johns, Terrance G TG; Boyd, Andrew W AW
Publication Date: 2019-03-20

Variant appearance in text: rs10406069
PubMed Link: 30894629
Variant Present in the following documents:
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 5
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 8
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 2
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 13
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 10
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 12
View BVdb publication page



Variants in the 14q32 miRNA cluster are associated with osteosarcoma risk in the Spanish population.

Scientific Reports
Martin-Guerrero, Idoia I; Bilbao-Aldaiturriaga, Nerea N; Gutierrez-Camino, Angela A; Santos-Zorrozua, Borja B; Dolžan, Vita V; Patiño-Garcia, Ana A; Garcia-Orad, Africa A
Publication Date: 2018-10-18

Variant appearance in text: rs10406069
PubMed Link: 30337581
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_33712.pdf
View BVdb publication page



Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: rs10406069
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



SNP Regulation of microRNA Expression and Subsequent Colon Cancer Risk.

Plos One
Mullany, Lila E LE; Wolff, Roger K RK; Herrick, Jennifer S JS; Buas, Matthew F MF; Slattery, Martha L ML
Publication Date: 2015

Variant appearance in text: rs10406069
PubMed Link: 26630397
Variant Present in the following documents:
  • Main text
  • pone.0143894.pdf
View BVdb publication page



Pharmacogenomics of estrogens on changes in carotid artery intima-medial thickness and coronary arterial calcification: Kronos Early Estrogen Prevention Study.

Physiological Genomics
Miller, Virginia M VM; Jenkins, Gregory D GD; Biernacka, Joanna M JM; Heit, John A JA; Huggins, Gordon S GS; Hodis, Howard N HN; Budoff, Matthew J MJ; Lobo, Rogerio A RA; Taylor, Hugh S HS; Manson, JoAnn E JE; Black, Dennis M DM; Naftolin, Frederick F; Harman, S Mitchell SM; de Andrade, Mariza M
Publication Date: 2016-01

Variant appearance in text: rs10406069
PubMed Link: 26508701
Variant Present in the following documents:
  • Main text
View BVdb publication page



Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.

Scientific Reports
Steinberg, Karyn Meltz KM; Yu, Bing B; Koboldt, Daniel C DC; Mardis, Elaine R ER; Pamphlett, Roger R
Publication Date: 2015-03-16

Variant appearance in text: rs10406069
PubMed Link: 25773295
Variant Present in the following documents:
  • srep09124-s2.xls, sheet 1
View BVdb publication page



The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.

Nucleic Acids Research
Tang, Xiaojia X; Baheti, Saurabh S; Shameer, Khader K; Thompson, Kevin J KJ; Wills, Quin Q; Niu, Nifang N; Holcomb, Ilona N IN; Boutet, Stephane C SC; Ramakrishnan, Ramesh R; Kachergus, Jennifer M JM; Kocher, Jean-Pierre A JP; Weinshilboum, Richard M RM; Wang, Liewei L; Thompson, E Aubrey EA; Kalari, Krishna R KR
Publication Date: 2014-12-16

Variant appearance in text: rs10406069
PubMed Link: 25352556
Variant Present in the following documents:
  • supp_gku1005_nar-01266-met-n-2014-File012.xlsx, sheet 23
View BVdb publication page



Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19.

Bmc Medical Genetics
Lillvis, John H JH; Kyo, Yoshiki Y; Tromp, Gerard G; Lenk, Guy M GM; Li, Ming M; Lu, Qing Q; Igo, Robert P RP; Sakalihasan, Natzi N; Ferrell, Robert E RE; Schworer, Charles M CM; Gatalica, Zoran Z; Land, Susan S; Kuivaniemi, Helena H
Publication Date: 2011-01-19

Variant appearance in text: rs10406069
PubMed Link: 21247474
Variant Present in the following documents:
  • Main text
  • 1471-2350-12-14.pdf
View BVdb publication page