Variant #0000887106 (NC_000006.11:g.157099408_157099425dup, NM_020732.3:c.345_362dup (ARID1B))

Chromosome 6
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.157099408_157099425dup
DNA change (hg38) -
Published as ARID1B(NM_001371656.1):c.594_611dupGCAGCAGCAGCAGCAGCA (p.Q209_Q214dup)
ISCN -
DB-ID ARID1B_000399
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 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARID1B NM_001374828.1 -?/. - c.594_611dup r.(?) p.(Gln209_Gln214dup)
ARID1B NM_020732.3 -?/. - c.345_362dup r.(?) p.(Gln126_Gln131dup)


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