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ABCA4 c.3342_3344del ;(p.I1114del)
Variant ID: 1-94506942-CATG-C
NM_000350.2(
ABCA4
):c.3342_3344del;(p.I1114del)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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: Ile1114del
PubMed Link:
36566289
Variant Present in the following documents:
Main text
41598_2022_Article_26912.pdf
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: 3342_3344delCAT
PubMed Link:
31814693
Variant Present in the following documents:
Main text
mv-v25-679.pdf
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: 3342_3344delCAT; I1114_M1115delinsM
PubMed Link:
31144483
Variant Present in the following documents:
Main text
jkms-34-e161.pdf
View BVdb publication page