Variant #0000718545 (NC_000002.11:g.227661003C>G, NM_005544.2:c.2452G>C (IRS1))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.227661003C>G |
DNA change (hg38) |
- |
Published as |
IRS1(NM_005544.2):c.2452G>C (p.(Gly818Arg), p.G818R), IRS1(NM_005544.3):c.2452G>C (p.G818R) |
ISCN |
- |
DB-ID |
IRS1_000007 See all 3 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.0084 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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