Variant #0001053106 (NC_000008.10:g.120844749C>A, NM_003184.3:c.56G>T (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.120844749C>A
DNA change (hg38) -
Published as TAF2(NM_003184.4):c.56G>T (p.(Gly19Val))
ISCN -
DB-ID DSCC1_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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 ?/. - c.56G>T r.(?) p.(Gly19Val)
DSCC1 NM_024094.2 ?/. - c.*2384G>T r.(=) p.(=)


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