TPRN c.1232_1233delinsAG ;(p.I411K)

Variant ID: 9-140093931-AA-CT

NM_001128228.2(TPRN):c.1232_1233delinsAG;(p.I411K)

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:

A combined genome-wide association and molecular study of age-related hearing loss in H. sapiens.

Bmc Medicine
Liu, Wei W; Johansson, Åsa Å; Rask-Andersen, Helge H; Rask-Andersen, Mathias M
Publication Date: 2021-12-01

Variant appearance in text: TPRN: I411K
PubMed Link: 34847940
Variant Present in the following documents:
  • 12916_2021_Article_2169.pdf
View BVdb publication page


A combined genome-wide association and molecular study of age-related hearing loss in H. sapiens.

Bmc Medicine
Liu, Wei W; Johansson, Åsa Å; Rask-Andersen, Helge H; Rask-Andersen, Mathias M
Publication Date: 2021-12-01

Variant appearance in text: TPRN: I411K
PubMed Link: 34847940
Variant Present in the following documents:
  • 12916_2021_Article_2169.pdf
View BVdb publication page