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THSD7A c.1076A>G ;(p.K359R)
Variant ID: 7-11633076-T-C
NM_015204.2(
THSD7A
):c.1076A>G;(p.K359R)
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: THSD7A: 1076A>G; Lys359Arg
PubMed Link:
29104234
Variant Present in the following documents:
cells-06-00040-s001.pdf
View BVdb publication page