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KCNQ1 c.160_161insATCGCGCCC ;(p.I54delinsNRAL)
Variant ID: 11-2466488-A-AATCGCGCCC
NM_000218.2(
KCNQ1
):c.160_161insATCGCGCCC;(p.I54delinsNRAL)
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:
Atrial fibrillation: the role of common and rare genetic variants.
European Journal Of Human Genetics : Ejhg
Olesen, Morten S MS; Nielsen, Morten W MW; Haunsø, Stig S; Svendsen, Jesper H JH
Publication Date: 2014-03
Variant appearance in text: KCNQ1: 160_168insATCGCGCCC
PubMed Link:
23838598
Variant Present in the following documents:
Main text
View BVdb publication page