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THSD7A c.667G>A ;(p.A223T)
Variant ID: 7-11676112-C-T
NM_015204.2(
THSD7A
):c.667G>A;(p.A223T)
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:
Modelling mutational landscapes of human cancers in vitro.
Scientific Reports
Olivier, Magali M; Weninger, Annette A; Ardin, Maude M; Huskova, Hana H; Castells, Xavier X; Vallée, Maxime P MP; McKay, James J; Nedelko, Tatiana T; Muehlbauer, Karl-Rudolf KR; Marusawa, Hiroyuki H; Alexander, John J; Hazelwood, Lee L; Byrnes, Graham G; Hollstein, Monica M; Zavadil, Jiri J
Publication Date: 2014-03-27
Variant appearance in text: THSD7A: A223T
PubMed Link:
24670820
Variant Present in the following documents:
srep04482-s4.xls, sheet 18
View BVdb publication page