Variant #0000831939 (NC_000014.8:g.76437977del, NM_003239.2:c.437del (TGFB3))
| Chromosome |
14 |
| 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.76437977del |
| DNA change (hg38) |
g.75971634del |
| Published as |
c.437delT |
| ISCN |
- |
| DB-ID |
TGFB3_000086 |
| Variant remarks |
ACMG PM2, PVS1, PP3 |
| 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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