Variant #0000831914 (NC_000001.10:g.218520337_218520351del, NM_003238.3:c.294_308del (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.218520337_218520351del
DNA change (hg38) g.218346995_218347009del
Published as c.294_308delCTACGCCAAGGAGGT
ISCN -
DB-ID TGFB2_000068
Variant remarks ACMG PM2, PP3, PM4, 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.294_308del r.(?) p.(Ala100_Tyr104del)


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