Variant #0000868867 (NC_000011.9:g.2154842A>G, IGF2(NM_000612.4):c.211T>C)

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.2154842A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID IGF2_000028 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1564894932
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGF2 NM_000612.4 +/. - c.211T>C r.(?) p.(Cys71Arg)