USH2A c.14527A>G ;(p.R4843G)

Variant ID: 1-215821925-T-C

NM_206933.2(USH2A):c.14527A>G;(p.R4843G)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome.

Human Genetics
Tollefson, Mallory R MR; Gogal, Rose A RA; Weaver, A Monique AM; Schaefer, Amanda M AM; Marini, Robert J RJ; Azaiez, Hela H; Kolbe, Diana L DL; Wang, Donghong D; Weaver, Amy E AE; Casavant, Thomas L TL; Braun, Terry A TA; Smith, Richard J H RJH; Schnieders, Michael J MJ
Publication Date: 2023-04-22

Variant appearance in text: USH2A: 14527A>G; Arg4843Gly
PubMed Link: 37086329
Variant Present in the following documents:
  • 439_2023_2559_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Novel biallelic USH2A variants in a patient with usher syndrome type IIA- a case report.

Bmc Ophthalmology
Young, Su Ling SL; Stanton, Chloe M CM; Livesey, Benjamin J BJ; Marsh, Joseph A JA; Cackett, Peter D PD
Publication Date: 2022-03-26

Variant appearance in text: rs910691220
PubMed Link: 35346118
Variant Present in the following documents:
  • 12886_2022_2353_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Natural and cryptic peptides dominate the immunopeptidome of atypical teratoid rhabdoid tumors.

Journal For Immunotherapy Of Cancer
Marcu, Ana A; Schlosser, Andreas A; Keupp, Anne A; Trautwein, Nico N; Johann, Pascal P; Wölfl, Matthias M; Lager, Johanna J; Monoranu, Camelia Maria CM; Walz, Juliane S JS; Henkel, Lisa M LM; Krauß, Jürgen J; Ebinger, Martin M; Schuhmann, Martin M; Thomale, Ulrich Wilhelm UW; Pietsch, Torsten T; Klinker, Erdwine E; Schlegel, Paul G PG; Oyen, Florian F; Reisner, Yair Y; Rammensee, Hans-Georg HG; Eyrich, Matthias M
Publication Date: 2021-10

Variant appearance in text: USH2A: R4843G
PubMed Link: 34599019
Variant Present in the following documents:
  • jitc-2021-003404supp008.pdf
View BVdb publication page



Targeted next generation sequencing in Italian patients with Usher syndrome: phenotype-genotype correlations.

Scientific Reports
Eandi, Chiara M CM; Dallorto, Laura L; Spinetta, Roberta R; Micieli, Maria Pia MP; Vanzetti, Mario M; Mariottini, Alessandro A; Passerini, Ilaria I; Torricelli, Francesca F; Alovisi, Camilla C; Marchese, Cristiana C
Publication Date: 2017-11-15

Variant appearance in text: USH2: Arg4843Gly
PubMed Link: 29142287
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_16014.pdf
View BVdb publication page