Variant #0000163731 (NC_000012.11:g.102813415C>T, IGF1(NM_000618.3):c.274G>A)
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 4 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 International |
Created by |
Johan den Dunnen |

Variant on transcripts
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