Variant #0001057091 (NC_000022.10:g.24129357A>G, NM_003073.3:c.1A>G (SMARCB1))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24129357A>G
DNA change (hg38) -
Published as SMARCB1(NM_003073.5):c.1A>G (p.(Met1?))
ISCN -
DB-ID DERL3_000030
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) 0.00015 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCB1 NM_003073.3 -?/. - c.1A>G r.(?) p.?
MMP11 NM_005940.3 -?/. - c.*3626A>G r.(=) p.(=)
DERL3 NM_198440.3 -?/. - c.*49890T>C r.(=) p.(=)


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