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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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