ABCA4 c.5196+899C>T

Variant ID: 1-94484239-G-A

NM_000350.2(ABCA4):c.5196+899C>T

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06

Variant appearance in text: ABCA4: 5196+899C>T; rs145838948
PubMed Link: 33503336
Variant Present in the following documents:
  • CNR2-4-e1335-s003.xlsx, sheet 2
  • CNR2-4-e1335-s003.xlsx, sheet 1
View BVdb publication page



Detailed Phenotyping and Therapeutic Strategies for Intronic ABCA4 Variants in Stargardt Disease.

Molecular Therapy. Nucleic Acids
Khan, Mubeen M; Arno, Gavin G; Fakin, Ana A; Parfitt, David A DA; Dhooge, Patty P A PPA; Albert, Silvia S; Bax, Nathalie M NM; Duijkers, Lonneke L; Niblock, Michael M; Hau, Kwan L KL; Bloch, Edward E; Schiff, Elena R ER; Piccolo, Davide D; Hogden, Michael C MC; Hoyng, Carel B CB; Webster, Andrew R AR; Cremers, Frans P M FPM; Cheetham, Michael E ME; Garanto, Alejandro A; Collin, Rob W J RWJ
Publication Date: 2020-09-04

Variant appearance in text: ABCA4: 5196+899C>T
PubMed Link: 32653833
Variant Present in the following documents:
  • Main text
  • main.pdf
  • mmc6.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: ABCA4: 5196+899C>T
PubMed Link: 28118664
Variant Present in the following documents:
  • iovs-57-15-69_s04.pdf
View BVdb publication page



Identification of Novel Mutations in ABCA4 Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease.

Biomed Research International
Battu, Rajani R; Verma, Anshuman A; Hariharan, Ramesh R; Krishna, Shuba S; Kiran, Ravi R; Jacob, Jemima J; Ganapathy, Aparna A; Ramprasad, Vedam L VL; Kumaramanickavel, Govindasamy G; Jeyabalan, Nallathambi N; Ghosh, Arkasubhra A
Publication Date: 2015

Variant appearance in text: ABCA4: 5196+899C>T; rs145838948
PubMed Link: 25922843
Variant Present in the following documents:
  • Main text
  • BMRI2015-940864.pdf
View BVdb publication page