ABCA4 c.5513A>G ;(p.H1838R)

Variant ID: 1-94476889-T-C

NM_000350.2(ABCA4):c.5513A>G;(p.H1838R)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Functional Characterization of ABCA4 Missense Variants Linked to Stargardt Macular Degeneration.

International Journal Of Molecular Sciences
Garces, Fabian A FA; Scortecci, Jessica F JF; Molday, Robert S RS
Publication Date: 2020-12-27

Variant appearance in text: ABCA4: H1838R
PubMed Link: 33375396
Variant Present in the following documents:
  • Main text
  • ijms-22-00185.pdf
View BVdb publication page



58th Annual Symposium of the International Society for Clinical Electrophysiology of Vision (ISCEV 2020) : 14-16 September 2020.

Documenta Ophthalmologica. Advances In Ophthalmology
Publication Date: 2020-09

Variant appearance in text: ABCA4: His1838Arg
PubMed Link: 32915376
Variant Present in the following documents:
  • 10633_2020_Article_9789.pdf
View BVdb publication page



Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs.

Investigative Ophthalmology & Visual Science
Schulz, Heidi L HL; Grassmann, Felix F; Kellner, Ulrich U; Spital, Georg G; Rüther, Klaus K; Jägle, Herbert H; Hufendiek, Karsten K; Rating, Philipp P; Huchzermeyer, Cord C; Baier, Maria J MJ; Weber, Bernhard H F BH; Stöhr, Heidi H
Publication Date: 2017-01-01

Variant appearance in text: STGD: 5513A>G
PubMed Link: 28118664
Variant Present in the following documents:
  • iovs-57-15-69_s05.pdf
  • iovs-57-15-69_s04.pdf
View BVdb publication page