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

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
Date created 2009-08-18 09:11:52 +02:00 (CEST)
Date last edited N/A
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.(=)


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