Bibliome.ai browser hg19
Search
About
Stats
FAQ
TLN2 c.7G>A ;(p.A3T)
Variant ID: 15-62939516-G-A
NM_015059.2(
TLN2
):c.7G>A;(p.A3T)
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:
Dupuytren's and Ledderhose Diseases in a Family with LMNA-Related Cardiomyopathy and a Novel Variant in the ASTE1 Gene.
Cells
Zaragoza, Michael V MV; Nguyen, Cecilia H H CHH; Widyastuti, Halida P HP; McCarthy, Linda A LA; Grosberg, Anna A
Publication Date: 2017-11-01
Variant appearance in text: TLN2: 7G>A; Ala3Thr
PubMed Link:
29104234
Variant Present in the following documents:
cells-06-00040-s001.pdf
View BVdb publication page