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DMD c.697_698delinsCA ;(p.T233Q)
Variant ID: X-32717362-GT-TG
NM_004006.2(
DMD
):c.697_698delinsCA;(p.T233Q)
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:
Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.
Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09
Variant appearance in text: DMD: T233Q
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page
Development of Patient-specific AAV Vectors After Neutralizing Antibody Selection for Enhanced Muscle Gene Transfer.
Molecular Therapy : The Journal Of The American Society Of Gene Therapy
Li, Chengwen C; Wu, Shuqing S; Albright, Blake B; Hirsch, Matthew M; Li, Wuping W; Tseng, Yu-Shan YS; Agbandje-McKenna, Mavis M; McPhee, Scott S; Asokan, Aravind A; Samulski, R Jude RJ
Publication Date: 2016-02
Variant appearance in text: DMD: T233Q
PubMed Link:
26220272
Variant Present in the following documents:
Main text
View BVdb publication page