Variant #0000913140 (NC_000009.11:g.2039818_2039820dup, NM_003070.3:c.708_710dup (SMARCA2))

Chromosome 9
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.2039818_2039820dup
DNA change (hg38) -
Published as SMARCA2(NM_003070.3):c.708_710dupACA (p.(Gln237dup)), SMARCA2(NM_003070.5):c.708_710dupACA (p.Q238dup)
ISCN -
DB-ID SMARCA2_000180 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) 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 2023-01-11 15:44:22 +01:00 (CET)
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     
SMARCA2 NM_003070.3 ?/. - c.708_710dup r.(?) p.(Gln238dup)


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