Variant #0000831917 (NC_000001.10:g.218520348_218520350del, NM_003238.3:c.305_307del (TGFB2))

Chromosome 1
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.218520348_218520350del
DNA change (hg38) g.218347006_218347008del
Published as c.305_307delAGG
ISCN -
DB-ID TGFB2_000071
Variant remarks ACMG PM2, PM4, 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGFB2 NM_003238.3 +?/. - c.305_307del r.(?) p.(Glu102del)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.