Bibliome.ai browser hg19
Search
About
Stats
FAQ
KMT2C c.4035G>T ;(p.K1345N)
Variant ID: 7-151900076-C-A
NM_170606.2(
KMT2C
):c.4035G>T;(p.K1345N)
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:
Clinical characteristics and genetic analysis of gene mutations in a Chinese pedigree with Peutz-Jeghers syndrome.
Clinical Case Reports
Qiu, Yudian Y; Xuan, Tao T; Yin, Mujun M; Gao, Zhidong Z; Guo, Peng P; Chen, Xi X; Ye, Yingjiang Y; Shen, Zhanlong Z
Publication Date: 2019-04
Variant appearance in text: MLL3: 4035G>T
PubMed Link:
30997075
Variant Present in the following documents:
Main text
CCR3-7-735.pdf
View BVdb publication page