USH2A c.8917_8918del ;(p.L2973Kfs*79)

Variant ID: 1-216019302-TAG-T

NM_206933.2(USH2A):c.8917_8918del;(p.L2973Kfs*79)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


The genetic landscape of inherited retinal dystrophies in Arabs.

Bmc Medical Genomics
Jaffal, Lama L; Joumaa, Hawraa H; Noureldine, Jinane J; Banjak, Malak M; Ibrahim, Mariam M; Mrad, Zamzam Z; Salami, Ali A; Shamieh, Said El SE
Publication Date: 2023-05-01

Variant appearance in text: USH2A: 8917_8918del; Leu2973Lysfs
PubMed Link: 37127645
Variant Present in the following documents:
  • 12920_2023_1518_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal Dystrophies.

Genes
Azab, Bilal B; Dardas, Zain Z; Aburizeg, Dunia D; Al-Bdour, Muawyah M; Abu-Ameerh, Mohammed M; Saleh, Tareq T; Barham, Raghda R; Maswadi, Ranad R; Ababneh, Nidaa A NA; Alsalem, Mohammad M; Zouk, Hana H; Amr, Sami S; Awidi, Abdalla A
Publication Date: 2021-04-19

Variant appearance in text: USH2A: 8917_8918del; Leu2973Lysfs
PubMed Link: 33921607
Variant Present in the following documents:
  • Main text
View BVdb publication page



Comprehensive genomic diagnosis of inherited retinal and optical nerve disorders reveals hidden syndromes and personalized therapeutic options.

Acta Ophthalmologica
Diñeiro, Marta M; Capín, Raquel R; Cifuentes, Guadalupe Á GÁ; Fernández-Vega, Beatriz B; Villota, Eva E; Otero, Andrea A; Santiago, Adrián A; Pruneda, Patricia C PC; Castillo, David D; Viejo-Díaz, Mónica M; Hernando, Inés I; Durán, Noelia S NS; Álvarez, Rebeca R; Lago, Claudia G CG; Ordóñez, Gonzalo R GR; Fernández-Vega, Álvaro Á; Cabanillas, Rubén R; Cadiñanos, Juan J
Publication Date: 2020-12

Variant appearance in text: USH2A: 8917_8918delCT; Leu2973Lysfs*79
PubMed Link: 32483926
Variant Present in the following documents:
  • Main text
  • AOS-98-e1034-s006.xlsx, sheet 1
View BVdb publication page