Variant #0000831925 (NC_000001.10:g.218609452C>T, NM_003238.3:c.895C>T (TGFB2))
Chromosome |
1 |
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.218609452C>T |
DNA change (hg38) |
g.218436110C>T |
Published as |
NM_001135599.2:c.979C>T |
ISCN |
- |
DB-ID |
TGFB2_000022 See all 6 reported entries |
Variant remarks |
ACMG PM2, PS1, PM5, PP3, PM1, PP1-S |
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
|