Variant #0000866742 (NC_000022.10:g.24158969C>T, NM_003073.3:c.641C>T (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.24158969C>T
DNA change (hg38) -
Published as SMARCB1(NM_003073.3):c.641C>T (p.(Thr214Met)), SMARCB1(NM_003073.5):c.641C>T (p.T214M)
ISCN -
DB-ID DERL3_000015 See all 2 reported entries
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 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.641C>T r.(?) p.(Thr214Met)
DERL3 NM_198440.3 ?/. - c.*20278G>A r.(=) p.(=)


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