ABCA4 c.1989G>A ;(p.W663*)

Variant ID: 1-94526264-C-T

NM_000350.2(ABCA4):c.1989G>A;(p.W663*)

This variant was identified in 7 publications

View GRCh38 version.




Publications:


A genotype-phenotype correlation matrix for ABCA4 disease based on long-term prognostic outcomes.

Jci Insight
Lee, Winston W; Zernant, Jana J; Su, Pei-Yin PY; Nagasaki, Takayuki T; Tsang, Stephen H SH; Allikmets, Rando R
Publication Date: 2022-01-25

Variant appearance in text: ABCA4: Trp663*
PubMed Link: 34874912
Variant Present in the following documents:
  • jciinsight-7-156154.pdf
View BVdb publication page



Retinal Pigment Epithelium Atrophy in Recessive Stargardt Disease as Measured by Short-Wavelength and Near-Infrared Autofluorescence.

Translational Vision Science & Technology
Jauregui, Ruben R; Nuzbrokh, Yan Y; Su, Pei-Yin PY; Zernant, Jana J; Allikmets, Rando R; Tsang, Stephen H SH; Sparrow, Janet R JR
Publication Date: 2021-01

Variant appearance in text: ABCA4: W663*
PubMed Link: 33505770
Variant Present in the following documents:
  • tvst-10-1-3_s002.pdf
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: W663X
PubMed Link: 32884132
Variant Present in the following documents:
  • NIHMS1630822-supplement-Supplementary_Tables.xlsx, sheet 6
View BVdb publication page



Multi-platform imaging in ABCA4-Associated Disease.

Scientific Reports
Chen, Lijuan L; Lee, Winston W; de Carvalho, Jose Ronaldo Lima JRL; Chang, Stanley S; Tsang, Stephen H SH; Allikmets, Rando R; Sparrow, Janet R JR
Publication Date: 2019-04-23

Variant appearance in text: ABCA4: W663*
PubMed Link: 31015497
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_42772.pdf
View BVdb publication page



Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting.

American Journal Of Human Genetics
Wright, Caroline F CF; West, Ben B; Tuke, Marcus M; Jones, Samuel E SE; Patel, Kashyap K; Laver, Thomas W TW; Beaumont, Robin N RN; Tyrrell, Jessica J; Wood, Andrew R AR; Frayling, Timothy M TM; Hattersley, Andrew T AT; Weedon, Michael N MN
Publication Date: 2019-02-07

Variant appearance in text: ABCA4: W663X
PubMed Link: 30665703
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence in Stargardt Disease.

Investigative Ophthalmology & Visual Science
Greenstein, Vivienne C VC; Nunez, Jason J; Lee, Winston W; Schuerch, Kaspar K; Fortune, Brad B; Tsang, Stephen H SH; Allikmets, Rando R; Sparrow, Janet R JR; Hood, Donald C DC
Publication Date: 2017-10-01

Variant appearance in text: ABCA4: W663*
PubMed Link: 29049723
Variant Present in the following documents:
  • i1552-5783-58-12-5227.pdf
View BVdb publication page



Familial discordance in Stargardt disease.

Molecular Vision
Burke, Tomas R TR; Tsang, Stephen H SH; Zernant, Jana J; Smith, R Theodore RT; Allikmets, Rando R
Publication Date: 2012

Variant appearance in text: ABCA4: W663X
PubMed Link: 22312191
Variant Present in the following documents:
  • Main text
  • mv-v18-227.pdf
View BVdb publication page