Variant #0000658451 (NC_000019.9:g.11097217_11097228dup, NM_003072.3:c.708_719dup (SMARCA4))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11097217_11097228dup
DNA change (hg38) g.10986541_10986552dup
Published as SMARCA4(NM_001128844.3):c.708_719dupTGGCCCCGGCCC (p.G241_P244dup)
ISCN -
DB-ID SMARCA4_000130
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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCA4 NM_003072.3 -?/. - c.708_719dup r.(?) p.(Gly241_Pro244dup)


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