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MAML2 c.1328G>A ;(p.R443H)
Variant ID: 11-95825867-C-T
NM_032427.1(
MAML2
):c.1328G>A;(p.R443H)
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:
Recurrent PDGFRB mutations in unicentric Castleman disease.
Leukemia
Li, Zhaoming Z; Lan, Xuan X; Li, Chaoping C; Zhang, Yanjie Y; Wang, Yingjun Y; Xue, Weili W; Lu, Lisha L; Jin, Mengyuan M; Zhou, Zhiyuan Z; Wang, Xinhua X; Li, Ling L; Zhang, Lei L; Li, Xin X; Fu, Xiaorui X; Sun, Zhenchang Z; Wu, Jingjing J; Zhang, Xudong X; Yu, Hui H; Nan, Feifei F; Chang, Yu Y; Yan, Jiaqin J; Wu, Xiaolong X; Wang, Guannan G; Zhang, Dandan D; Zhang, Yuan Y; Young, Ken H KH; Zhang, Mingzhi M
Publication Date: 2019-04
Variant appearance in text: MAML2: R443H
PubMed Link:
30607019
Variant Present in the following documents:
41375_2018_323_MOESM5_ESM.xls, sheet 2
View BVdb publication page