Variant #0000831922 (NC_000001.10:g.218607723C>A, NM_003238.3:c.687C>A (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.218607723C>A
DNA change (hg38) g.218434381C>A
Published as NM_001135599.2:c.687C>A
ISCN -
DB-ID TGFB2_000075
Variant remarks ACMG PM2, PVS1, PP3, PP1, 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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-01-01 13:58:51 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGFB2 NM_003238.3 +/. - c.687C>A p.Cys229* p.(Cys229*)


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