VCAN c.9265+1G>T

Variant ID: 5-82838088-G-T

NM_004385.4(VCAN):c.9265+1G>T

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics
Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P
Publication Date: 2023-02-23

Variant appearance in text: VCAN: 9265+1G>T
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



Regulatory RNA binding proteins contribute to the transcriptome-wide splicing alterations in human cellular senescence.

Aging
Dong, Qiongye Q; Wei, Lei L; Zhang, Michael Q MQ; Wang, Xiaowo X
Publication Date: 2018-06-24

Variant appearance in text: VCAN: 9265+1G>T; rs80356553
PubMed Link: 29936497
Variant Present in the following documents:
  • aging-10-101485-s002.xlsx, sheet 10
View BVdb publication page



Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome.

Archives Of Ophthalmology (Chicago, Ill. : 1960)
Ronan, Shawn M SM; Tran-Viet, Khanh-Nhat KN; Burner, Erica L EL; Metlapally, Ravikanth R; Toth, Cynthia A CA; Young, Terri L TL
Publication Date: 2009-11

Variant appearance in text: CSPG2: 9265+1G>T
PubMed Link: 19901218
Variant Present in the following documents:
  • Main text
View BVdb publication page