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 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     

P-domain     
TGFB3 NM_003239.2 +/. - c.437del r.(?) p.(Leu146HisfsTer68) -


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