ABCA4 c.3420C>G ;(p.C1140W)

Variant ID: 1-94506867-G-C

NM_000350.2(ABCA4):c.3420C>G;(p.C1140W)

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Functional characterization of ABCA4 genetic variants related to Stargardt disease.

Scientific Reports
Kim, Bo Min BM; Song, Hyo Sook HS; Kim, Jin-Young JY; Kwon, Eun Young EY; Ha, Seung Yeon SY; Kim, Minsuk M; Choi, Ji Ha JH
Publication Date: 2022-12-24

Variant appearance in text: ABCA4: Cys1140Trp
PubMed Link: 36566289
Variant Present in the following documents:
  • Main text
  • 41598_2022_26912_MOESM1_ESM.pdf
  • 41598_2022_Article_26912.pdf
View BVdb publication page



Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4-Related Retinopathy: Deep Intronic Variants and Copy Number Variations.

Investigative Ophthalmology & Visual Science
Tian, Lu L; Chen, Chunjie C; Song, Yuning Y; Zhang, Xiaohui X; Xu, Ke K; Xie, Yue Y; Jin, Zi-Bing ZB; Li, Yang Y
Publication Date: 2022-06-01

Variant appearance in text: STGD: 3420C>G
PubMed Link: 35657619
Variant Present in the following documents:
  • iovs-63-6-5_s002.xlsx, sheet 2
  • iovs-63-6-5_s002.xlsx, sheet 1
View BVdb publication page



Impact of Next Generation Sequencing in Unraveling the Genetics of 1036 Spanish Families With Inherited Macular Dystrophies.

Investigative Ophthalmology & Visual Science
Del Pozo-Valero, Marta M; Riveiro-Alvarez, Rosa R; Martin-Merida, Inmaculada I; Blanco-Kelly, Fiona F; Swafiri, Saoud S; Lorda-Sanchez, Isabel I; Trujillo-Tiebas, Maria José MJ; Carreño, Ester E; Jimenez-Rolando, Belen B; Garcia-Sandoval, Blanca B; Corton, Marta M; Avila-Fernandez, Almudena A; Ayuso, Carmen C
Publication Date: 2022-02-01

Variant appearance in text: ABCA4: 3420C>G
PubMed Link: 35119454
Variant Present in the following documents:
  • iovs-63-2-11_s003.pdf
View BVdb publication page



Impact of Next Generation Sequencing in Unraveling the Genetics of 1036 Spanish Families With Inherited Macular Dystrophies.

Investigative Ophthalmology & Visual Science
Del Pozo-Valero, Marta M; Riveiro-Alvarez, Rosa R; Martin-Merida, Inmaculada I; Blanco-Kelly, Fiona F; Swafiri, Saoud S; Lorda-Sanchez, Isabel I; Trujillo-Tiebas, Maria José MJ; Carreño, Ester E; Jimenez-Rolando, Belen B; Garcia-Sandoval, Blanca B; Corton, Marta M; Avila-Fernandez, Almudena A; Ayuso, Carmen C
Publication Date: 2022-02-01

Variant appearance in text: ABCA4: 3420C>G
PubMed Link: 35119454
Variant Present in the following documents:
  • iovs-63-2-11_s003.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: C1140W
PubMed Link: 32884132
Variant Present in the following documents:
  • NIHMS1630822-supplement-Supplementary_Tables.xlsx, sheet 6
View BVdb publication page



Genotypic profile and phenotype correlations of ABCA4-associated retinopathy in Koreans.

Molecular Vision
Joo, Kwangsic K; Seong, Moon-Woo MW; Park, Kyu Hyung KH; Park, Sung Sup SS; Woo, Se Joon SJ
Publication Date: 2019

Variant appearance in text: STGD: 3420C>G
PubMed Link: 31814693
Variant Present in the following documents:
  • Main text
  • mv-v25-679.pdf
View BVdb publication page



ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants.

Frontiers In Genetics
Hu, Fang-Yuan FY; Li, Jian-Kang JK; Gao, Feng-Juan FJ; Qi, Yu-He YH; Xu, Ping P; Zhang, Yong-Jin YJ; Wang, Dan-Dan DD; Wang, Lu-Sheng LS; Li, Wei W; Wang, Min M; Chen, Fang F; Shen, Si-Mai SM; Xu, Ge-Zhi GZ; Zhang, Sheng-Hai SH; Chang, Qing Q; Wu, Ji-Hong JH
Publication Date: 2019

Variant appearance in text: STGD1: 3420C>G
PubMed Link: 31543898
Variant Present in the following documents:
  • Table_3.xls, sheet 1
  • Table_2.xls, sheet 1
View BVdb publication page



Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases.

Journal Of Korean Medical Science
Kim, Min Seok MS; Joo, Kwangsic K; Seong, Moon Woo MW; Kim, Man Jin MJ; Park, Kyu Hyung KH; Park, Sung Sup SS; Woo, Se Joon SJ
Publication Date: 2019-06-02

Variant appearance in text: ABCA4: 3420C>G
PubMed Link: 31144483
Variant Present in the following documents:
  • Main text
  • jkms-34-e161.pdf
View BVdb publication page



Molecular diagnosis of putative Stargardt disease by capture next generation sequencing.

Plos One
Zhang, Xiao X; Ge, Xianglian X; Shi, Wei W; Huang, Ping P; Min, Qingjie Q; Li, Minghan M; Yu, Xinping X; Wu, Yaming Y; Zhao, Guangyu G; Tong, Yi Y; Jin, Zi-Bing ZB; Qu, Jia J; Gu, Feng F
Publication Date: 2014

Variant appearance in text: ABCA4: 3420C>G
PubMed Link: 24763286
Variant Present in the following documents:
  • Main text
  • pone.0095528.pdf
View BVdb publication page