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RUNX2 c.263C>A ;(p.A88D)
Variant ID: 6-45390534-C-A
NM_001024630.3(
RUNX2
):c.263C>A;(p.A88D)
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:
Establishment of a human induced pluripotent stem cell neuronal model for identification of modulators of A53T α-synuclein levels and aggregation.
Plos One
Vajhøj, Charlotte C; Schmid, Benjamin B; Alik, Ania A; Melki, Ronald R; Fog, Karina K; Holst, Bjørn B; Stummann, Tina Charlotte TC
Publication Date: 2021
Variant appearance in text: CCD: A88D
PubMed Link:
34932569
Variant Present in the following documents:
Main text
View BVdb publication page
Implementing an intermittent spin-coating strategy to enable bottom-up crystallization in layered halide perovskites.
Nature Communications
Yan, Yajie Y; Yang, Yingguo Y; Liang, Mingli M; Abdellah, Mohamed M; Pullerits, Tõnu T; Zheng, Kaibo K; Liang, Ziqi Z
Publication Date: 2021-11-15
Variant appearance in text: CCD: A88D
PubMed Link:
34782603
Variant Present in the following documents:
Main text
View BVdb publication page
The rate of compensatory mutation in the DNA bacteriophage phiX174.
Genetics
Poon, Art A; Chao, Lin L
Publication Date: 2005-07
Variant appearance in text: CCD: A88D
PubMed Link:
15911582
Variant Present in the following documents:
Main text
View BVdb publication page