Variant #0000128819 (NC_000011.9:g.2168147C>T, IGF2(NM_000612.4):c.-8695G>A)

Chromosome 11
Allele Parent #1
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.2168147C>T
DNA change (hg38) g.2146917C>T
Published as -
ISCN -
DB-ID IGF2_000002
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs17883917
Origin Germline
Segregation -
Frequency 0.00-0.05
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGF2 NM_000612.4 ?/. _1 c.-8695G>A r.(?) p.(=)