SI c.343_345delinsCAA ;(p.N115Q)

Variant ID: 3-164786894-GTT-TTG

NM_001041.3(SI):c.343_345delinsCAA;(p.N115Q)

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:

HPMPdb: A machine learning-ready database of protein molecular phenotypes associated to human missense variants.

Current Research In Structural Biology
Raimondi, Daniele D; Codicè, Francesco F; Orlando, Gabriele G; Schymkowitz, Joost J; Rousseau, Frederic F; Moreau, Yves Y
Publication Date: 2022

Variant appearance in text: SI: N115Q
PubMed Link: 35669450
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page