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AMACR c.1001_1002delinsAG ;(p.T334K)
Variant ID: 5-33989345-GG-CT
NM_014324.5(
AMACR
):c.1001_1002delinsAG;(p.T334K)
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 reveals damaging gene variants associated with hypoalphalipoproteinemia.
Journal Of Lipid Research
Dong, Weilai W; Wong, Karen H Y KHY; Liu, Youbin Y; Levy-Sakin, Michal M; Hung, Wei-Chien WC; Li, Mo M; Li, Boyang B; Jin, Sheng Chih SC; Choi, Jungmin J; Lopez-Giraldez, Francesc F; Vaka, Dedeepya D; Poon, Annie A; Chu, Catherine C; Lao, Richard R; Balamir, Melek M; Movsesyan, Irina I; Malloy, Mary J MJ; Zhao, Hongyu H; Kwok, Pui-Yan PY; Kane, John P JP; Lifton, Richard P RP; Pullinger, Clive R CR
Publication Date: 2022-06
Variant appearance in text: AMACR: Thr334Lys
PubMed Link:
35460704
Variant Present in the following documents:
mmc1.pdf
View BVdb publication page
The evolving proteome of SARS-CoV-2 predominantly uses mutation combination strategy for survival.
Computational And Structural Biotechnology Journal
Patro, L Ponoop Prasad LPP; Sathyaseelan, Chakkarai C; Uttamrao, Patil Pranita PP; Rathinavelan, Thenmalarchelvi T
Publication Date: 2021
Variant appearance in text: P504S: T334K
PubMed Link:
34109017
Variant Present in the following documents:
mmc6.xlsx, sheet 1
mmc10.xlsx, sheet 1
View BVdb publication page