Variant #0000254851 (NC_000022.10:g.24143206A>G, NM_003073.3:c.438A>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.24143206A>G
DNA change (hg38) g.23801019A>G
Published as SMARCB1(NM_003073.3):c.438A>G (p.P146=)
ISCN -
DB-ID SMARCB1_000048
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) 0.00126 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-17 11:34:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCB1 NM_003073.3 -?/. - c.438A>G r.(?) p.(Pro146=)
DERL3 NM_198440.3 -?/. - c.*36041T>C r.(=) p.(=)


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