ACVRL1 c.142G>A ;(p.G48R)

Variant ID: 12-52306963-G-A

NM_000020.2(ACVRL1):c.142G>A;(p.G48R)

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: HHT2: G48R
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: ACVRL1: G48R
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Specificity and structure of a high affinity activin receptor-like kinase 1 (ALK1) signaling complex.

The Journal Of Biological Chemistry
Townson, Sharon A SA; Martinez-Hackert, Erik E; Greppi, Chloe C; Lowden, Patricia P; Sako, Dianne D; Liu, June J; Ucran, Jeffrey A JA; Liharska, Katia K; Underwood, Kathryn W KW; Seehra, Jasbir J; Kumar, Ravindra R; Grinberg, Asya V AV
Publication Date: 2012-08-10

Variant appearance in text: HHT2: G48R
PubMed Link: 22718755
Variant Present in the following documents:
  • Main text
View BVdb publication page



Bioinformatic analysis of pathogenic missense mutations of activin receptor like kinase 1 ectodomain.

Plos One
Scotti, Claudia C; Olivieri, Carla C; Boeri, Laura L; Canzonieri, Cecilia C; Ornati, Federica F; Buscarini, Elisabetta E; Pagella, Fabio F; Danesino, Cesare C
Publication Date: 2011

Variant appearance in text: HHT2: G48R
PubMed Link: 22028876
Variant Present in the following documents:
  • Main text
  • pone.0026431.pdf
View BVdb publication page



Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations.

Journal Of Medical Genetics
Prigoda, N L NL; Savas, S S; Abdalla, S A SA; Piovesan, B B; Rushlow, D D; Vandezande, K K; Zhang, E E; Ozcelik, H H; Gallie, B L BL; Letarte, M M
Publication Date: 2006-09

Variant appearance in text: N/A
PubMed Link: 16690726
Variant Present in the following documents:
View BVdb publication page



Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease.

Journal Of Medical Genetics
Abdalla, S A SA; Letarte, M M
Publication Date: 2006-02

Variant appearance in text:
PubMed Link: 15879500
Variant Present in the following documents:
  • Main text
View BVdb publication page