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THSD7A c.3364G>A ;(p.V1122M)
Variant ID: 7-11464342-C-T
NM_015204.2(
THSD7A
):c.3364G>A;(p.V1122M)
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:
Genetic variants in African-American and Hispanic patients with breast cancer.
Oncology Letters
Dutta, Pranabananda P; Keung, Man Y MY; Wu, Yanyuan Y; Vadgama, Jaydutt V JV
Publication Date: 2023-02
Variant appearance in text: THSD7A: 3364G>A; V1122M
PubMed Link:
36644153
Variant Present in the following documents:
Supplementary_Data5.xlsx, sheet 2
View BVdb publication page
Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.
Scientific Reports
Steinberg, Karyn Meltz KM; Yu, Bing B; Koboldt, Daniel C DC; Mardis, Elaine R ER; Pamphlett, Roger R
Publication Date: 2015-03-16
Variant appearance in text: THSD7A: V1122M
PubMed Link:
25773295
Variant Present in the following documents:
srep09124-s3.xls, sheet 1
View BVdb publication page