Variant #0000308619 (NC_000022.10:g.24129568_24129569del, NC_000022.10(NM_003073.3):c.93+119_93+120del (SMARCB1))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24129568_24129569del
DNA change (hg38) g.23787381_23787382del
Published as SMARCB1(NM_003073.3):c.93+119_93+120delGC
ISCN -
DB-ID SMARCB1_000041
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCB1 NM_003073.3 -/. - c.93+119_93+120del r.(=) p.(=)
MMP11 NM_005940.3 -/. - c.*3837_*3838del r.(=) p.(=)
DERL3 NM_198440.3 -/. - c.*49692_*49693del r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.