Variant #0000850062 (NC_000002.11:g.8931339_8931340dup, NM_020738.2:c.1291_1292dup (KIDINS220))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.8931339_8931340dup
DNA change (hg38) -
Published as KIDINS220(NM_001348738.2):c.1291_1292dupAC (p.E432Lfs*49)
ISCN -
DB-ID KIDINS220_000045
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIDINS220 NM_020738.2 ?/. - c.1291_1292dup r.(?) p.(Glu432Leufs*49)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.