MAPK1 c.*1037T>G

Variant ID: 22-22117502-A-C

NM_002745.5(MAPK1):c.*1037T>G

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?

European Journal Of Human Genetics : Ejhg
Ferrari, Luca L; Mangano, Eleonora E; Bonati, Maria Teresa MT; Monterosso, Ilaria I; Capitanio, Daniele D; Chiappori, Federica F; Brambilla, Ilaria I; Gelfi, Cecilia C; Battaglia, Cristina C; Bordoni, Roberta R; Riva, Paola P
Publication Date: 2020-10

Variant appearance in text: rs13058
PubMed Link: 32514133
Variant Present in the following documents:
  • 41431_2020_658_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



A Bioinformatics Approach to Prioritize Single Nucleotide Polymorphisms in TLRs Signaling Pathway Genes.

International Journal Of Molecular And Cellular Medicine
Alipoor, Behnam B; Ghaedi, Hamid H; Omrani, Mir Davood MD; Bastami, Milad M; Meshkani, Reza R; Golmohammadi, Taghi T
Publication Date: 2016

Variant appearance in text: rs13058
PubMed Link: 27478803
Variant Present in the following documents:
  • Main text
  • ijmcm-5-065.pdf
View BVdb publication page



Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio
Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M
Publication Date: 2014

Variant appearance in text: rs13058
PubMed Link: 24490137
Variant Present in the following documents:
  • mmc5.xlsx, sheet 2
View BVdb publication page



Transcriptome-wide analysis of UTRs in non-small cell lung cancer reveals cancer-related genes with SNV-induced changes on RNA secondary structure and miRNA target sites.

Plos One
Sabarinathan, Radhakrishnan R; Wenzel, Anne A; Novotny, Peter P; Tang, Xiaojia X; Kalari, Krishna R KR; Gorodkin, Jan J
Publication Date: 2014

Variant appearance in text: rs13058
PubMed Link: 24416147
Variant Present in the following documents:
  • Main text
  • pone.0082699.s005.xlsx, sheet 1
  • pone.0082699.pdf
View BVdb publication page



Functional polymorphisms in the serotonin 1B receptor gene (HTR1B) predict self-reported anger and hostility among young men.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Conner, Tamlin S TS; Jensen, Kevin P KP; Tennen, Howard H; Furneaux, Henry M HM; Kranzler, Henry R HR; Covault, Jonathan J
Publication Date: 2010-01-05

Variant appearance in text: rs13058
PubMed Link: 19350534
Variant Present in the following documents:
  • Main text
View BVdb publication page