CMYA5 c.11689+799A>G

Variant ID: 5-79085726-A-G

NM_153610.3(CMYA5):c.11689+799A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Pushing the Boundaries: Forensic DNA Phenotyping Challenged by Single-Cell Sequencing.

Genes
Diepenbroek, Marta M; Bayer, Birgit B; Anslinger, Katja K
Publication Date: 2021-08-30

Variant appearance in text: rs12657828
PubMed Link: 34573344
Variant Present in the following documents:
  • genes-12-01362.pdf
View BVdb publication page



DCDC2 READ1 regulatory element: how temporal processing differences may shape language.

Proceedings. Biological Sciences
Tang, Kevin K; DeMille, Mellissa M C MMC; Frijters, Jan C JC; Gruen, Jeffrey R JR
Publication Date: 2020-06-10

Variant appearance in text: rs12657828
PubMed Link: 32486976
Variant Present in the following documents:
  • rspb20192712supp1.pdf
View BVdb publication page



Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes.

Journal Of Thrombosis And Haemostasis : Jth
de Haan, H G HG; van Hylckama Vlieg, A A; Lotta, L A LA; Gorski, M M MM; Bucciarelli, P P; Martinelli, I I; Baglin, T P TP; Peyvandi, F F; Rosendaal, F R FR; ,
Publication Date: 2018-12

Variant appearance in text: rs12657828
PubMed Link: 30168256
Variant Present in the following documents:
  • NIHMS1021906-supplement-1.pdf
View BVdb publication page