DDX3Y c.674-52A>C

Variant ID: Y-15026424-A-C

NM_004660.3(DDX3Y):c.674-52A>C

This variant was identified in 8 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: rs2032624
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



The genomic ancestry of the Scandinavian Battle Axe Culture people and their relation to the broader Corded Ware horizon.

Proceedings. Biological Sciences
Malmström, Helena H; Günther, Torsten T; Svensson, Emma M EM; Juras, Anna A; Fraser, Magdalena M; Munters, Arielle R AR; Pospieszny, Łukasz Ł; Tõrv, Mari M; Lindström, Jonathan J; Götherström, Anders A; Storå, Jan J; Jakobsson, Mattias M
Publication Date: 2019-10-09

Variant appearance in text: rs2032624
PubMed Link: 31594508
Variant Present in the following documents:
  • rspb20191528supp1.pdf
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs2032624
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 3
View BVdb publication page



Blind study evaluation illustrates utility of the Ion PGM™ system for use in human identity DNA typing.

Croatian Medical Journal
Churchill, Jennifer D JD; Chang, Joseph J; Ge, Jianye J; Rajagopalan, Narasimhan N; Wootton, Sharon C SC; Chang, Chien-Wei CW; Lagacé, Robert R; Liao, Wenchi W; King, Jonathan L JL; Budowle, Bruce B
Publication Date: 2015-06

Variant appearance in text: rs2032624
PubMed Link: 26088846
Variant Present in the following documents:
  • Main text
  • CroatMedJ_56_0218.pdf
View BVdb publication page



Genetic polymorphism of human Y chromosome and risk factors for cardiovascular diseases: a study in WOBASZ cohort.

Plos One
Kostrzewa, Grażyna G; Broda, Grażyna G; Konarzewska, Magdalena M; Krajewki, Paweł P; Płoski, Rafał R
Publication Date: 2013

Variant appearance in text: rs2032624
PubMed Link: 23935855
Variant Present in the following documents:
  • Main text
  • pone.0068155.pdf
View BVdb publication page



Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry.

Human Genetics
Wang, Zhaoming Z; Parikh, Hemang H; Jia, Jinping J; Myers, Timothy T; Yeager, Meredith M; Jacobs, Kevin B KB; Hutchinson, Amy A; Burdett, Laurie L; Ghosh, Arpita A; Thun, Michael J MJ; Gapstur, Susan M SM; Ryan Diver, W W; Virtamo, Jarmo J; Albanes, Demetrius D; Cancel-Tassin, Geraldine G; Valeri, Antoine A; Cussenot, Olivier O; Offit, Kenneth K; Giovannucci, Ed E; Ma, Jing J; Stampfer, Meir J MJ; Michael Gaziano, J J; Hunter, David J DJ; Dutra-Clarke, Ana A; Kirchhoff, Tomas T; Alavanja, Michael M; Freeman, Laura B LB; Koutros, Stella S; Hoover, Robert R; Berndt, Sonja I SI; Hayes, Richard B RB; Agalliu, Ilir I; Burk, Robert D RD; Wacholder, Sholom S; Thomas, Gilles G; Amundadottir, Laufey L
Publication Date: 2012-07

Variant appearance in text: rs2032624
PubMed Link: 22271044
Variant Present in the following documents:
  • Main text
View BVdb publication page



People of the British Isles: preliminary analysis of genotypes and surnames in a UK-control population.

European Journal Of Human Genetics : Ejhg
Winney, Bruce B; Boumertit, Abdelhamid A; Day, Tammy T; Davison, Dan D; Echeta, Chikodi C; Evseeva, Irina I; Hutnik, Katarzyna K; Leslie, Stephen S; Nicodemus, Kristin K; Royrvik, Ellen C EC; Tonks, Susan S; Yang, Xiaofeng X; Cheshire, James J; Longley, Paul P; Mateos, Pablo P; Groom, Alexandra A; Relton, Caroline C; Bishop, D Tim DT; Black, Kathryn K; Northwood, Emma E; Parkinson, Louise L; Frayling, Timothy M TM; Steele, Anna A; Sampson, Julian R JR; King, Turi T; Dixon, Ron R; Middleton, Derek D; Jennings, Barbara B; Bowden, Rory R; Donnelly, Peter P; Bodmer, Walter W
Publication Date: 2012-02

Variant appearance in text: rs2032624
PubMed Link: 21829225
Variant Present in the following documents:
  • Main text
  • ejhg2011127a.pdf
View BVdb publication page



Genetic variation in South Indian castes: evidence from Y-chromosome, mitochondrial, and autosomal polymorphisms.

Bmc Genetics
Watkins, W S WS; Thara, R R; Mowry, B J BJ; Zhang, Y Y; Witherspoon, D J DJ; Tolpinrud, W W; Bamshad, M J MJ; Tirupati, S S; Padmavati, R R; Smith, H H; Nancarrow, D D; Filippich, C C; Jorde, L B LB
Publication Date: 2008-12-12

Variant appearance in text: rs2032624
PubMed Link: 19077280
Variant Present in the following documents:
  • 1471-2156-9-86-S1.xls, sheet 1
View BVdb publication page