Variant #0001046807 (NC_000022.10:g.24145490_24145493dup, NM_003073.3:c.509_512dup (SMARCB1))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.24145490_24145493dup
DNA change (hg38) -
Published as SMARCB1(NM_003073.5):c.509_512dupACCA (p.H171Qfs*3)
ISCN -
DB-ID DERL3_000029
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCB1 NM_003073.3 +/. - c.509_512dup r.(?) p.(His171Glnfs*3)
DERL3 NM_198440.3 +/. - c.*33754_*33757dup r.(=) p.(=)


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