Variant #0001074028 (NC_000020.10:g.60640865_60640887del, NM_003185.3:c.-13_10del (TAF4))

Chromosome 20
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.60640865_60640887del
DNA change (hg38) -
Published as -
ISCN -
DB-ID TAF4_000031
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2516042500
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-17 12:03:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF4 NM_003185.3 ?/. - c.-13_10del r.(?) p.(?)


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