USH2A c.10252_10254del ;(p.F3418del)

Variant ID: 1-215960144-TGAA-T

NM_206933.2(USH2A):c.10252_10254del;(p.F3418del)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Variant analysis of 92 Chinese Han families with hearing loss.

Bmc Medical Genomics
Jin, Xiaohua X; Huang, Shasha S; An, Lisha L; Zhang, Chuan C; Dai, Pu P; Gao, Huafang H; Ma, Xu X
Publication Date: 2022-01-21

Variant appearance in text: USH2A: 10251_10253del
PubMed Link: 35062939
Variant Present in the following documents:
  • 12920_2022_Article_1158.pdf
View BVdb publication page


Variant analysis of 92 Chinese Han families with hearing loss.

Bmc Medical Genomics
Jin, Xiaohua X; Huang, Shasha S; An, Lisha L; Zhang, Chuan C; Dai, Pu P; Gao, Huafang H; Ma, Xu X
Publication Date: 2022-01-21

Variant appearance in text: USH2A: 10251_10253del
PubMed Link: 35062939
Variant Present in the following documents:
  • 12920_2022_Article_1158.pdf
View BVdb publication page