Variant #0000163731 (NC_000012.11:g.102813415C>T, NM_000618.3:c.274G>A (IGF1))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.102813415C>T
DNA change (hg38) g.102419637C>T
Published as V44M
ISCN -
DB-ID IGF1_000003 See all 5 reported entries
Variant remarks cDNA expression cloning showed 90x reduced affinity for IGF1R
Reference -
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
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 2017-03-10 15:09:53 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGF1 NM_000618.3 +/. 4 c.274G>A r.(?) p.Val92Met
IGF1 NM_001111283.1 ./. - c.? - -


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