DNAH11 c.11425_11427delinsTGT ;(p.R3809C)

Variant ID: 7-21904204-CGA-TGT

NM_001277115.1(DNAH11):c.11425_11427delinsTGT;(p.R3809C)

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:

An association-adjusted consensus deleterious scheme to classify homozygous Mis-sense mutations for personal genome interpretation.

Biodata Mining
Preeprem, Thanawadee T; Gibson, Greg G
Publication Date: 2013-12-23

Variant appearance in text: DNAH11: R3809C
PubMed Link: 24365473
Variant Present in the following documents:
  • 1756-0381-6-24-S2.xlsx, sheet 6
View BVdb publication page