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MTHFD2 c.*3062A>T
Variant ID: 2-74444431-A-T
NM_006636.3(
MTHFD2
):c.*3062A>T
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:
Non-syndromic Cleft Palate: An Overview on Human Genetic and Environmental Risk Factors.
Frontiers In Cell And Developmental Biology
Martinelli, Marcella M; Palmieri, Annalisa A; Carinci, Francesco F; Scapoli, Luca L
Publication Date: 2020
Variant appearance in text: rs702462
PubMed Link:
33195260
Variant Present in the following documents:
Main text
fcell-08-592271.pdf
View BVdb publication page
Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.
Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10
Variant appearance in text: rs702462
PubMed Link:
29221171
Variant Present in the following documents:
oncotarget-08-95841-s002.xlsx, sheet 1
oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page
Investigating the complex genetic architecture of ankle-brachial index, a measure of peripheral arterial disease, in non-Hispanic whites.
Bmc Medical Genomics
Kardia, Sharon Lr SL; Greene, M Todd MT; Boerwinkle, Eric E; Turner, Stephen T ST; Kullo, Iftikhar J IJ
Publication Date: 2008-05-15
Variant appearance in text: rs702462
PubMed Link:
18482449
Variant Present in the following documents:
Main text
1755-8794-1-16.pdf
View BVdb publication page