Variant #0000913534 (NC_000011.9:g.17409283dup, KCNJ11(NM_000525.3):c.356dup)

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.17409283dup
DNA change (hg38) -
Published as KCNJ11(NM_000525.4):c.356dupC (p.A120Cfs*7)
ISCN -
DB-ID KCNJ11_000076 See all 2 reported entries
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNJ11 NM_000525.3 +/. - c.356dup r.(?) p.(Ala120Cysfs*7)