Variant #0001022240 (NC_000008.10:g.120773964C>G, NC_000008.10(NM_003184.3):c.2558+691G>C (TAF2))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.120773964C>G
DNA change (hg38) g.119761724C>G
Published as -
ISCN -
DB-ID TAF2_000021 See all 2 reported entries
Variant remarks in vitro analysis 293T cells mini-gene exon trapping assay: variant activates pseudoexon
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Tjakko van Ham
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-11-05 16:15:00 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF2 NM_003184.3 ?/. 19i c.2558+691G>C r.[2558_2559ins[2558+643_2558+690;C;2558+692_2558+807],=] p.Ser253ProfsTer23


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