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PSEN1 c.1166A>C ;(p.Y389S)
Variant ID: 14-73683870-A-C
NM_000021.3(
PSEN1
):c.1166A>C;(p.Y389S)
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:
A Novel Probable Pathogenic PSEN2 Mutation p.Phe369Ser Associated With Early-Onset Alzheimer's Disease in a Chinese Han Family: A Case Report.
Frontiers In Aging Neuroscience
Wan, Ke K; Ma, Zhen-Juan ZJ; Zhou, Xia X; Zhang, Yi-Mei YM; Yu, Xian-Feng XF; You, Meng-Zhe MZ; Huang, Chao-Juan CJ; Zhang, Wei W; Sun, Zhong-Wu ZW
Publication Date: 2021
Variant appearance in text: PSEN1: Tyr389Ser
PubMed Link:
34366829
Variant Present in the following documents:
Main text
fnagi-13-710075.pdf
View BVdb publication page
PSEN1 variants in Korean patients with clinically suspicious early-onset familial Alzheimer's disease.
Scientific Reports
Kim, Young-Eun YE; Cho, Hanna H; Kim, Hee Jin HJ; Na, Duk L DL; Seo, Sang Won SW; Ki, Chang-Seok CS
Publication Date: 2020-02-26
Variant appearance in text: PSEN1: Tyr389Ser
PubMed Link:
32103039
Variant Present in the following documents:
Main text
41598_2020_Article_59829.pdf
View BVdb publication page