ABCA4 c.5312+2T>G

Variant ID: 1-94481293-A-C

NM_000350.2(ABCA4):c.5312+2T>G

This variant was identified in 4 publications

View GRCh38 version.




Publications:


The prevalence, genetic complexity and population-specific founder effects of human autosomal recessive disorders.

Npj Genomic Medicine
Xiao, Qingyang Q; Lauschke, Volker M VM
Publication Date: 2021-06-02

Variant appearance in text: ABCA4: 5312+2T>G; rs1307108997
PubMed Link: 34078906
Variant Present in the following documents:
  • 41525_2021_203_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



A novel statistical method for interpreting the pathogenicity of rare variants.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Wang, Jun J; Liu, Hehe H; Bertrand, Renae Elaine RE; Sarrion-Perdigones, Alejandro A; Gonzalez, Yezabel Y; Venken, Koen J T KJT; Chen, Rui R
Publication Date: 2021-01

Variant appearance in text: ABCA4: 5312+2T>G
PubMed Link: 32884132
Variant Present in the following documents:
  • NIHMS1630822-supplement-Supplementary_Tables.xlsx, sheet 6
View BVdb publication page



Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles.

International Journal Of Molecular Sciences
Ścieżyńska, Aneta A; Soszyńska, Marta M; Komorowski, Michał M; Podgórska, Anna A; Krześniak, Natalia N; Nogowska, Aleksandra A; Smolińska, Martyna M; Szulborski, Kamil K; Szaflik, Jacek P JP; Noszczyk, Bartłomiej B; Ołdak, Monika M; Malejczyk, Jacek J
Publication Date: 2020-05-13

Variant appearance in text: ABCA4: 5312+2T>G
PubMed Link: 32413971
Variant Present in the following documents:
  • Main text
  • ijms-21-03430.pdf
View BVdb publication page



Extremely hypomorphic and severe deep intronic variants in the ABCA4 locus result in varying Stargardt disease phenotypes.

Cold Spring Harbor Molecular Case Studies
Zernant, Jana J; Lee, Winston W; Nagasaki, Takayuki T; Collison, Frederick T FT; Fishman, Gerald A GA; Bertelsen, Mette M; Rosenberg, Thomas T; Gouras, Peter P; Tsang, Stephen H SH; Allikmets, Rando R
Publication Date: 2018-08

Variant appearance in text: ABCA4: 5312+2T>G
PubMed Link: 29848554
Variant Present in the following documents:
  • Main text
  • MCS002733Zer.pdf
View BVdb publication page