Variant #0000831837 (NC_000018.9:g.45374889A>T, NM_005901.5:c.954T>A (SMAD2))
Chromosome |
18 |
Allele |
Parent #1 |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45374889A>T |
DNA change (hg38) |
g.47848518A>T |
Published as |
- |
ISCN |
- |
DB-ID |
SMAD2_000035 |
Variant remarks |
ACMG PM2, PP3, PP2, PP1-M |
Reference |
PubMed: Schepers 2018 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
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 |
Date created |
2022-01-01 13:58:51 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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