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TENM4 c.3412G>T ;(p.V1138L)
Variant ID: 11-78437262-C-A
NM_001098816.2(
TENM4
):c.3412G>T;(p.V1138L)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics.
Scientific Reports
John, Sumi Elsa SE; Antony, Dinu D; Eaaswarkhanth, Muthukrishnan M; Hebbar, Prashantha P; Channanath, Arshad Mohamed AM; Thomas, Daisy D; Devarajan, Sriraman S; Tuomilehto, Jaakko J; Al-Mulla, Fahd F; Alsmadi, Osama O; Thanaraj, Thangavel Alphonse TA
Publication Date: 2018-11-08
Variant appearance in text: rs538881762
PubMed Link:
30409984
Variant Present in the following documents:
Main text
41598_2018_Article_34815.pdf
View BVdb publication page
Systematic analysis of genetic variants in patients with essential tremor.
Brain And Behavior
Yuan, Lamei L; Deng, Xiong X; Song, Zhi Z; Deng, Sheng S; Zheng, Wen W; Mao, Ping P; Deng, Hao H
Publication Date: 2018-10
Variant appearance in text: rs538881762
PubMed Link:
30252209
Variant Present in the following documents:
Main text
BRB3-8-e01100.pdf
View BVdb publication page
Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson's disease.
Scientific Reports
Yuan, Lamei L; Song, Zhi Z; Deng, Xiong X; Zheng, Wen W; Guo, Yi Y; Yang, Zhijian Z; Deng, Hao H
Publication Date: 2016-09-22
Variant appearance in text: rs538881762
PubMed Link:
27653456
Variant Present in the following documents:
Main text
srep33850-s1.pdf
srep33850.pdf
View BVdb publication page