Variant #0000831862 (NC_000015.9:g.67459123dup, NM_005902.3:c.539dup (SMAD3))
Chromosome |
15 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.67459123dup |
DNA change (hg38) |
g.67166785dup |
Published as |
c.539_540insC |
ISCN |
- |
DB-ID |
SMAD3_000116 See all 2 reported entries |
Variant remarks |
ACMG PM2, PVS1, PS1, PP4 |
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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