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CD4 c.1A>G ;(p.M1?)
Variant ID: 12-6909305-A-G
NM_000616.4(
CD4
):c.1A>G;(p.M1?)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder.
Ebiomedicine
Wang, Tao T; Zhao, Tingting T; Liu, Liqiu L; Teng, Huajing H; Fan, Tianda T; Li, Yi Y; Wang, Yan Y; Li, Jinchen J; Xia, Kun K; Sun, Zhongsheng Z
Publication Date: 2022-07
Variant appearance in text: CD4: 1A>G; M1V; rs200294737
PubMed Link:
35665681
Variant Present in the following documents:
mmc26.xlsx, sheet 1
View BVdb publication page
Idiopathic CD4+ Lymphocytopenia Due to Homozygous Loss of the CD4 Start Codon.
Cureus
Sama, Srikar S; Challa, Ashrit A; Patel, Foram V FV; Saineni, Sathvik S; Erpenwar, Sohan S; Maryala, Shashi S
Publication Date: 2021-05-26
Variant appearance in text: CD4: M1V
PubMed Link:
34188990
Variant Present in the following documents:
Main text
View BVdb publication page
Genetic variation in human drug-related genes.
Genome Medicine
Schärfe, Charlotta Pauline Irmgard CPI; Tremmel, Roman R; Schwab, Matthias M; Kohlbacher, Oliver O; Marks, Debora Susan DS
Publication Date: 2017-12-22
Variant appearance in text: rs200294737
PubMed Link:
29273096
Variant Present in the following documents:
13073_2017_502_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page