KIT c.1256_1257delinsGTCTA ;(p.D419delinsGL)

Variant ID: 4-55589774-AC-GTCTA

NM_000222.2(KIT):c.1256_1257delinsGTCTA;(p.D419delinsGL)

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:

INDELseek: detection of complex insertions and deletions from next-generation sequencing data.

Bmc Genomics
Au, Chun Hang CH; Leung, Anskar Y H AY; Kwong, Ava A; Chan, Tsun Leung TL; Ma, Edmond S K ES
Publication Date: 2017-01-05

Variant appearance in text: KIT: 1256_1257delinsGTCTA; Asp419delinsGlyLeu
PubMed Link: 28056804
Variant Present in the following documents:
  • Main text
  • 12864_2016_Article_3449.pdf
View BVdb publication page