KANSL1 c.*640T>C

Variant ID: 17-44108202-A-G

NM_015443.3(KANSL1):c.*640T>C

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs17574361
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs17574361
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs17574361
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
  • oncotarget-08-95841-s002.xlsx, sheet 1
View BVdb publication page



Human genetic variation and Parkinson's disease.

Journal Of Movement Disorders
Chung, Sun Ju SJ
Publication Date: 2010-05

Variant appearance in text: rs17574361
PubMed Link: 24868370
Variant Present in the following documents:
  • Main text
  • jmd-3-1-1-1.pdf
View BVdb publication page



Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.

Nature Communications
Permuth-Wey, Jennifer J; Lawrenson, Kate K; Shen, Howard C HC; Velkova, Aneliya A; Tyrer, Jonathan P JP; Chen, Zhihua Z; Lin, Hui-Yi HY; Chen, Y Ann YA; Tsai, Ya-Yu YY; Qu, Xiaotao X; Ramus, Susan J SJ; Karevan, Rod R; Lee, Janet J; Lee, Nathan N; Larson, Melissa C MC; Aben, Katja K KK; Anton-Culver, Hoda H; Antonenkova, Natalia N; Antoniou, Antonis C AC; Armasu, Sebastian M SM; , ; , ; Bacot, François F; Baglietto, Laura L; Bandera, Elisa V EV; Barnholtz-Sloan, Jill J; Beckmann, Matthias W MW; Birrer, Michael J MJ; Bloom, Greg G; Bogdanova, Natalia N; Brinton, Louise A LA; Brooks-Wilson, Angela A; Brown, Robert R; Butzow, Ralf R; Cai, Qiuyin Q; Campbell, Ian I; Chang-Claude, Jenny J; Chanock, Stephen S; Chenevix-Trench, Georgia G; Cheng, Jin Q JQ; Cicek, Mine S MS; Coetzee, Gerhard A GA; , ; Cook, Linda S LS; Couch, Fergus J FJ; Cramer, Daniel W DW; Cunningham, Julie M JM; Dansonka-Mieszkowska, Agnieszka A; Despierre, Evelyn E; Doherty, Jennifer A JA; Dörk, Thilo T; du Bois, Andreas A; Dürst, Matthias M; Easton, Douglas F DF; Eccles, Diana D; Edwards, Robert R; Ekici, Arif B AB; Fasching, Peter A PA; Fenstermacher, David A DA; Flanagan, James M JM; Garcia-Closas, Montserrat M; Gentry-Maharaj, Aleksandra A; Giles, Graham G GG; Glasspool, Rosalind M RM; Gonzalez-Bosquet, Jesus J; Goodman, Marc T MT; Gore, Martin M; Górski, Bohdan B; Gronwald, Jacek J; Hall, Per P; Halle, Mari K MK; Harter, Philipp P; Heitz, Florian F; Hillemanns, Peter P; Hoatlin, Maureen M; Høgdall, Claus K CK; Høgdall, Estrid E; Hosono, Satoyo S; Jakubowska, Anna A; Jensen, Allan A; Jim, Heather H; Kalli, Kimberly R KR; Karlan, Beth Y BY; Kaye, Stanley B SB; Kelemen, Linda E LE; Kiemeney, Lambertus A LA; Kikkawa, Fumitaka F; Konecny, Gottfried E GE; Krakstad, Camilla C; Kjaer, Susanne Krüger SK; Kupryjanczyk, Jolanta J; Lambrechts, Diether D; Lambrechts, Sandrina S; Lancaster, Johnathan M JM; Le, Nhu D ND; Leminen, Arto A; Levine, Douglas A DA; Liang, Dong D; Lim, Boon Kiong BK; Lin, Jie J; Lissowska, Jolanta J; Lu, Karen H KH; Lubiński, Jan J; Lurie, Galina G; Massuger, Leon F A G LF; Matsuo, Keitaro K; McGuire, Valerie V; McLaughlin, John R JR; Menon, Usha U; Modugno, Francesmary F; Moysich, Kirsten B KB; Nakanishi, Toru T; Narod, Steven A SA; Nedergaard, Lotte L; Ness, Roberta B RB; Nevanlinna, Heli H; Nickels, Stefan S; Noushmehr, Houtan H; Odunsi, Kunle K; Olson, Sara H SH; Orlow, Irene I; Paul, James J; Pearce, Celeste L CL; Pejovic, Tanja T; Pelttari, Liisa M LM; Pike, Malcolm C MC; Poole, Elizabeth M EM; Raska, Paola P; Renner, Stefan P SP; Risch, Harvey A HA; Rodriguez-Rodriguez, Lorna L; Rossing, Mary Anne MA; Rudolph, Anja A; Runnebaum, Ingo B IB; Rzepecka, Iwona K IK; Salvesen, Helga B HB; Schwaab, Ira I; Severi, Gianluca G; Shridhar, Viji V; Shu, Xiao-Ou XO; Shvetsov, Yurii B YB; Sieh, Weiva W; Song, Honglin H; Southey, Melissa C MC; Spiewankiewicz, Beata B; Stram, Daniel D; Sutphen, Rebecca R; Teo, Soo-Hwang SH; Terry, Kathryn L KL; Tessier, Daniel C DC; Thompson, Pamela J PJ; Tworoger, Shelley S SS; van Altena, Anne M AM; Vergote, Ignace I; Vierkant, Robert A RA; Vincent, Daniel D; Vitonis, Allison F AF; Wang-Gohrke, Shan S; Palmieri Weber, Rachel R; Wentzensen, Nicolas N; Whittemore, Alice S AS; Wik, Elisabeth E; Wilkens, Lynne R LR; Winterhoff, Boris B; Woo, Yin Ling YL; Wu, Anna H AH; Xiang, Yong-Bing YB; Yang, Hannah P HP; Zheng, Wei W; Ziogas, Argyrios A; Zulkifli, Famida F; Phelan, Catherine M CM; Iversen, Edwin E; Schildkraut, Joellen M JM; Berchuck, Andrew A; Fridley, Brooke L BL; Goode, Ellen L EL; Pharoah, Paul D P PD; Monteiro, Alvaro N A AN; Sellers, Thomas A TA; Gayther, Simon A SA
Publication Date: 2013

Variant appearance in text: rs17574361
PubMed Link: 23535648
Variant Present in the following documents:
  • Main text
  • nihms447293.pdf
View BVdb publication page



Cis-acting polymorphisms affect complex traits through modifications of microRNA regulation pathways.

Plos One
Arnold, Matthias M; Ellwanger, Daniel C DC; Hartsperger, Mara L ML; Pfeufer, Arne A; Stümpflen, Volker V
Publication Date: 2012

Variant appearance in text: rs17574361
PubMed Link: 22606281
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants in PARK loci and related genes and Parkinson's disease.

Movement Disorders : Official Journal Of The Movement Disorder Society
Chung, Sun Ju SJ; Armasu, Sebastian M SM; Biernacka, Joanna M JM; Lesnick, Timothy G TG; Rider, David N DN; Lincoln, Sarah J SJ; Ortolaza, Alexandra I AI; Farrer, Matthew J MJ; Cunningham, Julie M JM; Rocca, Walter A WA; Maraganore, Demetrius M DM
Publication Date: 2011-02-01

Variant appearance in text: rs17574361
PubMed Link: 21412835
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.

Nature Genetics
Hamza, Taye H TH; Zabetian, Cyrus P CP; Tenesa, Albert A; Laederach, Alain A; Montimurro, Jennifer J; Yearout, Dora D; Kay, Denise M DM; Doheny, Kimberly F KF; Paschall, Justin J; Pugh, Elizabeth E; Kusel, Victoria I VI; Collura, Randall R; Roberts, John J; Griffith, Alida A; Samii, Ali A; Scott, William K WK; Nutt, John J; Factor, Stewart A SA; Payami, Haydeh H
Publication Date: 2010-09

Variant appearance in text: rs17574361
PubMed Link: 20711177
Variant Present in the following documents:
  • NIHMS222438-supplement-1.pdf
View BVdb publication page