Variant #0000895612 (NC_000022.10:g.24129411C>A, NM_003073.3:c.55C>A (SMARCB1))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.24129411C>A
DNA change (hg38) -
Published as SMARCB1(NM_003073.5):c.55C>A (p.L19M)
ISCN -
DB-ID DERL3_000019
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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCB1 NM_003073.3 ?/. - c.55C>A r.(?) p.(Leu19Met)
MMP11 NM_005940.3 ?/. - c.*3680C>A r.(=) p.(=)
DERL3 NM_198440.3 ?/. - c.*49836G>T r.(=) p.(=)


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