Variant #0000831851 (NC_000015.9:g.67457326_67457327insAGGGCCGGCAGGC, NM_005902.3:c.300_301insAGGGCCGGCAGGC (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.67457326_67457327insAGGGCCGGCAGGC |
| DNA change (hg38) |
g.67164988_67164989insAGGGCCGGCAGGC |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SMAD3_000107 |
| Variant remarks |
ACMG PM2, PVS1, 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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