Variant #0000128817 (NC_000011.9:g.2166479A>G, IGF2(NM_000612.4):c.-7027T>C)

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.2166479A>G
DNA change (hg38) g.2145249A>G
Published as -
ISCN -
DB-ID IGF2_000003 See all 2 reported entries
Variant remarks Variant Error [EREF/ERANGE]: This genomic variant does not match the reference sequence; the transcript variant also has an error. Please fix this entry and then remove this message.
Reference -
ClinVar ID -
dbSNP ID rs3741211
Origin Germline
Segregation -
Frequency 0.25-0.53
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 ?/. 00-1i c.-7027T>C r.(?) p.(=)