DNAH11 c.1099_1100insATTA ;(p.T367Nfs*14)

Variant ID: 7-21603918-A-ATAAT

NM_001277115.1(DNAH11):c.1099_1100insATTA;(p.T367Nfs*14)

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 performance evaluation study: Variant annotation tools - the enigma of clinical next generation sequencing (NGS) based genetic testing.

Journal Of Pathology Informatics
Tuteja, Sachleen S; Kadri, Sabah S; Yap, Kai Lee KL
Publication Date: 2022

Variant appearance in text: DNAH11: 1099_1100insATTA; T367fs
PubMed Link: 36268089
Variant Present in the following documents:
  • main.pdf
View BVdb publication page