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THSD7A c.1529C>A ;(p.P510Q)
Variant ID: 7-11582669-G-T
NM_015204.2(
THSD7A
):c.1529C>A;(p.P510Q)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Currently favored sampling practices for tumor sequencing can produce optimal results in the clinical setting.
Scientific Reports
Pongor, Lőrinc S LS; Munkácsy, Gyöngyi G; Vereczkey, Ildikó I; Pete, Imre I; Győrffy, Balázs B
Publication Date: 2020-09-01
Variant appearance in text: THSD7A: 1529C>A; Pro510Gln
PubMed Link:
32873813
Variant Present in the following documents:
41598_2020_71382_MOESM6_ESM.xlsx, sheet 2
View BVdb publication page
Comprehensive genomic analysis of Oesophageal Squamous Cell Carcinoma reveals clinical relevance.
Scientific Reports
Du, Peina P; Huang, Peide P; Huang, Xuanlin X; Li, Xiangchun X; Feng, Zhimin Z; Li, Fengyu F; Liang, Shaoguang S; Song, Yongmei Y; Stenvang, Jan J; Brünner, Nils N; Yang, Huanming H; Ou, Yunwei Y; Gao, Qiang Q; Li, Lin L
Publication Date: 2017-11-10
Variant appearance in text: THSD7A: 1529C>A; P510Q
PubMed Link:
29127303
Variant Present in the following documents:
41598_2017_14909_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page