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PCSK9 c.1903T>C ;(p.C635R)
Variant ID: 1-55529081-T-C
NM_174936.3(
PCSK9
):c.1903T>C;(p.C635R)
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:
Patterns and tempo of PCSK9 pseudogenizations suggest an ancient divergence in mammalian cholesterol homeostasis mechanisms.
Genetica
van Asch, Barbara B; Teixeira da Costa, Luís Filipe LF
Publication Date: 2021-02
Variant appearance in text: PCSK9: Cys635Arg
PubMed Link:
33515402
Variant Present in the following documents:
Main text
10709_2021_Article_113.pdf
View BVdb publication page
The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.
Genes
Meshkov, Alexey A; Ershova, Alexandra A; Kiseleva, Anna A; Zotova, Evgenia E; Sotnikova, Evgeniia E; Petukhova, Anna A; Zharikova, Anastasia A; Malyshev, Pavel P; Rozhkova, Tatyana T; Blokhina, Anastasia A; Limonova, Alena A; Ramensky, Vasily V; Divashuk, Mikhail M; Khasanova, Zukhra Z; Bukaeva, Anna A; Kurilova, Olga O; Skirko, Olga O; Pokrovskaya, Maria M; Mikova, Valeriya V; Snigir, Ekaterina E; Akinshina, Alexsandra A; Mitrofanov, Sergey S; Kashtanova, Daria D; Makarov, Valentin V; Kukharchuk, Valeriy V; Boytsov, Sergey S; Yudin, Sergey S; Drapkina, Oxana O
Publication Date: 2021-01-06
Variant appearance in text: PCSK9: 1903T>C; Cys635Arg
PubMed Link:
33418990
Variant Present in the following documents:
Main text
genes-12-00066.pdf
View BVdb publication page