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MED23 c.4076A>C ;(p.Q1359P)
Variant ID: 6-131908850-T-G
NM_004830.3(
MED23
):c.4076A>C;(p.Q1359P)
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:
Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.
Molecular Neurobiology
Zhang, Yi Y; Wang, Tao T; Wang, Yan Y; Xia, Kun K; Li, Jinchen J; Sun, Zhongsheng Z
Publication Date: 2021-08
Variant appearance in text: MED23: 4076A>C; Q1359P
PubMed Link:
33860439
Variant Present in the following documents:
12035_2021_2377_MOESM12_ESM.xlsx, sheet 1
View BVdb publication page