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APP c.1735_1739del ;(p.N579Dfs*2)
Variant ID: 21-27284223-CATGTT-C
NM_000484.3(
APP
):c.1735_1739del;(p.N579Dfs*2)
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:
Genetic testing and clinical relevance of patients with thoracic aortic aneurysm and dissection in northwestern China.
Molecular Genetics & Genomic Medicine
Li, Jinjie J; Yang, Liu L; Diao, Yanjun Y; Zhou, Lei L; Xin, Yijuan Y; Jiang, Liqing L; Li, Rui R; Wang, Juan J; Duan, Weixun W; Liu, Jiayun J
Publication Date: 2021-10
Variant appearance in text: AD1: 1735_1739del
PubMed Link:
34498425
Variant Present in the following documents:
MGG3-9-e1800.pdf
View BVdb publication page
Genetic testing and clinical relevance of patients with thoracic aortic aneurysm and dissection in northwestern China.
Molecular Genetics & Genomic Medicine
Li, Jinjie J; Yang, Liu L; Diao, Yanjun Y; Zhou, Lei L; Xin, Yijuan Y; Jiang, Liqing L; Li, Rui R; Wang, Juan J; Duan, Weixun W; Liu, Jiayun J
Publication Date: 2021-10
Variant appearance in text: AD1: 1735_1739del
PubMed Link:
34498425
Variant Present in the following documents:
MGG3-9-e1800.pdf
View BVdb publication page