MSH2 c.*141T>G

Variant ID: 2-47710229-T-G

NM_000251.2(MSH2):c.*141T>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Somatic deletions of genes regulating MSH2 protein stability cause DNA mismatch repair deficiency and drug resistance in human leukemia cells.

Nature Medicine
Diouf, Barthelemy B; Cheng, Qing Q; Krynetskaia, Natalia F NF; Yang, Wenjian W; Cheok, Meyling M; Pei, Deqing D; Fan, Yiping Y; Cheng, Cheng C; Krynetskiy, Evgeny Y EY; Geng, Hui H; Chen, Siying S; Thierfelder, William E WE; Mullighan, Charles G CG; Downing, James R JR; Hsieh, Peggy P; Pui, Ching-Hon CH; Relling, Mary V MV; Evans, William E WE
Publication Date: 2011-09-25

Variant appearance in text: rs17225053
PubMed Link: 21946537
Variant Present in the following documents:
  • Main text
  • NIHMS309529-supplement-1.pdf
  • nihms-309529.pdf
View BVdb publication page