Bibliome.ai browser hg19
Search
About
Stats
FAQ
FNDC3B c.604C>A ;(p.R202S)
Variant ID: 3-171969145-C-A
NM_022763.3(
FNDC3B
):c.604C>A;(p.R202S)
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:
Whole-Exome Sequencing of Germline Variants in Non-BRCA Families with Hereditary Breast Cancer.
Biomedicines
Liu, Yaxuan Y; Helgadottir, Hafdis T HT; Kharaziha, Pedram P; Choi, Jungmin J; López-Giráldez, Francesc F; Mane, Shrikant M SM; Höiom, Veronica V; Juhlin, Carl Christofer CC; Larsson, Catharina C; Bajalica-Lagercrantz, Svetlana S
Publication Date: 2022-04-26
Variant appearance in text: rs190147254
PubMed Link:
35625741
Variant Present in the following documents:
biomedicines-10-01004.pdf
View BVdb publication page