ABCA4 c.1577A>C ;(p.E526A)

Variant ID: 1-94528851-T-G

NM_000350.2(ABCA4):c.1577A>C;(p.E526A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: E526A
PubMed Link: 32884132
Variant Present in the following documents:
  • NIHMS1630822-supplement-Supplementary_Tables.xlsx, sheet 6
View BVdb publication page



Recessive Stargardt disease phenocopying hydroxychloroquine retinopathy.

Graefe'S Archive For Clinical And Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie
Nõupuu, Kalev K; Lee, Winston W; Zernant, Jana J; Greenstein, Vivienne C VC; Tsang, Stephen S; Allikmets, Rando R
Publication Date: 2016-05

Variant appearance in text: ABCA4: E526A
PubMed Link: 26311262
Variant Present in the following documents:
  • Main text
View BVdb publication page