Variant #0000308606 (NC_000022.10:g.24176362T>G, NM_003073.3:c.1153T>G (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.24176362T>G
DNA change (hg38) g.23834175T>G
Published as SMARCB1(NM_003073.3):c.1153T>G (p.W385G)
ISCN -
DB-ID SMARCB1_000055
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_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCB1 NM_003073.3 +/. - c.1153T>G r.(?) p.(Trp385Gly)
DERL3 NM_198440.3 +/. - c.*2885A>C r.(=) p.(=)


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