Variant #0000831912 (NC_000001.10:g.218520287G>T, NM_003238.3:c.244G>T (TGFB2))

Chromosome 1
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.218520287G>T
DNA change (hg38) g.218346945G>T
Published as -
ISCN -
DB-ID TGFB2_000066
Variant remarks ACMG PM2, PP3, PP2, 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) 0 View details
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.244G>T r.(?) p.(Ala82Ser)


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