Variant #0000831909 (NC_000015.9:g.(?_67408242)_(67603013_?)del, NM_005902.3:c.(206+1_207-48991)_*4656{0} (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.(?_67408242)_(67603013_?)del |
| DNA change (hg38) |
- |
| Published as |
del ex2-9 |
| ISCN |
- |
| DB-ID |
SMAD3_000097 See all 3 reported entries |
| Variant remarks |
ACMG PVS1, PP3, PM2 |
| 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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