KIT c.265_266delinsTT ;(p.A89F)

Variant ID: 4-55561875-GC-TT

NM_000222.2(KIT):c.265_266delinsTT;(p.A89F)

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:

Persistent Human KIT Receptor Signaling Disposes Murine Placenta to Premature Differentiation Resulting in Severely Disrupted Placental Structure and Functionality.

International Journal Of Molecular Sciences
Kaiser, Franziska F; Hartweg, Julia J; Jansky, Selina S; Pelusi, Natalie N; Kubaczka, Caroline C; Sharma, Neha N; Nitsche, Dominik D; Langkabel, Jan J; Schorle, Hubert H
Publication Date: 2020-07-31

Variant appearance in text: KIT: A89F
PubMed Link: 32752102
Variant Present in the following documents:
  • Main text
View BVdb publication page