Variant #0000128818 (NC_000011.9:g.2168142T>C, NM_000612.4:c.-8690A>G (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.2168142T>C
DNA change (hg38) g.2146912T>C
Published as -
ISCN -
DB-ID IGF2_000001
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 rs10743144
Origin Germline
Segregation -
Frequency 0.00-0.12
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.-8690A>G r.(?) p.(=)


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