KMT2C c.11139C>T ;(p.A3713=)

Variant ID: 7-151859523-G-A

NM_170606.2(KMT2C):c.11139C>T;(p.A3713=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


RNA sequencing as an alternative tool for detecting measurable residual disease in core-binding factor acute myeloid leukemia.

Scientific Reports
Kim, TaeHyung T; Moon, Joon Ho JH; Ahn, Jae-Sook JS; Ahn, Seo-Yeon SY; Jung, Sung-Hoon SH; Yang, Deok-Hwan DH; Lee, Je-Jung JJ; Shin, Myung-Geun MG; Choi, Seung Hyun SH; Lee, Ja-Yeon JY; Tyndel, Marc S MS; Lee, Hui Young HY; Kim, Kyoung Ha KH; Cai, Yu Y; Lee, Yoo Jin YJ; Sohn, Sang Kyun SK; Min, Yoo Hong YH; Cheong, June-Won JW; Kim, Hyeoung-Joon HJ; Zhang, Zhaolei Z; Kim, Dennis Dong Hwan DDH
Publication Date: 2020-11-18

Variant appearance in text: KMT2C: A3713A
PubMed Link: 33208771
Variant Present in the following documents:
  • 41598_2020_76933_MOESM8_ESM.xlsx, sheet 4
View BVdb publication page