MLH1 c.1246A>T ;(p.K416*)

Variant ID: 3-37067335-A-T

NM_000249.3(MLH1):c.1246A>T;(p.K416*)

This variant was identified in 3 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: MLH1: 1246A>T; Lys416Ter
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: MLH1: 1246A>T; Lys416Ter
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 7
View BVdb publication page



Lynch syndrome among gynecologic oncology patients meeting Bethesda guidelines for screening.

Gynecologic Oncology
Walsh, Christine S CS; Blum, Audra A; Walts, Ann A; Alsabeh, Randa R; Tran, Hang H; Koeffler, H Phillip HP; Karlan, Beth Y BY
Publication Date: 2010-03

Variant appearance in text: MLH1: K416X
PubMed Link: 20034658
Variant Present in the following documents:
  • Main text
View BVdb publication page