KMT2D c.12304C>T ;(p.Q4102*)

Variant ID: 12-49426184-G-A

NM_003482.3(KMT2D):c.12304C>T;(p.Q4102*)

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: KMT2D: 12304C>T; Gln4102Ter
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM5_ESM.xlsx, sheet 4
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



Molecular subclusters of follicular lymphoma: a report from the United Kingdom's Haematological Malignancy Research Network.

Blood Advances
Crouch, Simon S; Painter, Daniel D; Barrans, Sharon L SL; Roman, Eve E; Beer, Philip A PA; Cooke, Susanna L SL; Glover, Paul P; Van Hoppe, Suzan J L SJL; Webster, Nichola N; Lacy, Stuart E SE; Ruiz, Camilo C; Campbell, Peter J PJ; Hodson, Daniel J DJ; Patmore, Russell R; Burton, Cathy C; Smith, Alexandra A; Tooze, Reuben M RM
Publication Date: 2022-11-08

Variant appearance in text: KMT2D: Q4102*
PubMed Link: 35363872
Variant Present in the following documents:
  • BLOODA_ADV-2021-005284-mmc1.xlsx, sheet 2
View BVdb publication page



Somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer.

Scientific Reports
Sakuta, Kazuhiro K; Sasaki, Yu Y; Abe, Yasuhiko Y; Sato, Hidenori H; Shoji, Masakuni M; Yaoita, Takao T; Yagi, Makoto M; Mizumoto, Naoko N; Onozato, Yusuke Y; Kon, Takashi T; Koseki, Ayumi A; Sato, Sonoko S; Murakami, Ryoko R; Miyano, Yuki Y; Ueno, Yoshiyuki Y
Publication Date: 2020-12-16

Variant appearance in text: KMT2D: Q4102X
PubMed Link: 33328548
Variant Present in the following documents:
  • 41598_2020_79195_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page



Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities.

European Journal Of Human Genetics : Ejhg
Sobreira, Nara N; Brucato, Martha M; Zhang, Li L; Ladd-Acosta, Christine C; Ongaco, Chrissie C; Romm, Jane J; Doheny, Kimberly F KF; Mingroni-Netto, Regina C RC; Bertola, Debora D; Kim, Chong A CA; Perez, Ana Ba AB; Melaragno, Maria I MI; Valle, David D; Meloni, Vera A VA; Bjornsson, Hans T HT
Publication Date: 2017-12

Variant appearance in text: KMT2D: 12304C>T
PubMed Link: 29255178
Variant Present in the following documents:
  • Main text
View BVdb publication page