Bibliome.ai browser hg19
Search
About
Stats
FAQ
SECISBP2 c.916C>G ;(p.Q306E)
Variant ID: 9-91949472-C-G
NM_024077.3(
SECISBP2
):c.916C>G;(p.Q306E)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia.
Bmc Medical Genomics
Lin, Dafeng D; Wang, Dianpeng D; Li, Peimao P; Deng, Lihua L; Zhang, Zhimin Z; Zhang, Yanfang Y; Zhang, Ming M; Zhang, Naixing N
Publication Date: 2023-01-26
Variant appearance in text: SECISBP2: 916C>G; Gln306Glu; rs752235357
PubMed Link:
36703207
Variant Present in the following documents:
12920_2023_1442_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page
Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities.
Frontiers In Genetics
Zhou, Yuan-Yuan YY; Du, Yu-Fang YF; Lu, Qing Q; Zhai, Xiu-Zhang XZ; Shi, Ming-Fang MF; Chen, Dan-Yun DY; Liu, Sun-Rong SR; Zhong, Ying Y
Publication Date: 2022
Variant appearance in text: SECISBP2: 916C>G; Gln306Glu; rs752235357
PubMed Link:
35464846
Variant Present in the following documents:
Table1.xlsx, sheet 1
View BVdb publication page