HP c.15A>T ;(p.G5=)

Variant ID: 16-72090069-A-T

NM_005143.3(HP):c.15A>T;(p.G5=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Association between reduced white matter integrity in the corpus callosum and serotonin transporter gene DNA methylation in medication-naive patients with major depressive disorder.

Translational Psychiatry
Won, E E; Choi, S S; Kang, J J; Kim, A A; Han, K-M KM; Chang, H S HS; Tae, W S WS; Son, K R KR; Joe, S-H SH; Lee, M-S MS; Ham, B-J BJ
Publication Date: 2016-08-09

Variant appearance in text: HP: G5=
PubMed Link: 27505229
Variant Present in the following documents:
  • Main text
View BVdb publication page



Characterization of a novel large deletion caused by double-stranded breaks in 6-bp microhomologous sequences of intron 11 and 12 of the F13A1 gene.

Human Genome Variation
Thomas, Anne A; Ivaškevičius, Vytautas V; Zawadzki, Christophe C; Goudemand, Jenny J; Biswas, Arijit A; Oldenburg, Johannes J
Publication Date: 2016

Variant appearance in text: HP: g5=
PubMed Link: 27081562
Variant Present in the following documents:
  • hgv201559.pdf
View BVdb publication page