Variant #0000331295 (NC_000006.11:g.157100005_157100007dup, NM_020732.3:c.942_944dup (ARID1B))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.157100005_157100007dup
DNA change (hg38) g.156778871_156778873dup
Published as ARID1B(NM_001374828.1):c.1191_1193dup (p.(Gly402dup)), ARID1B(NM_020732.3):c.942_944dupCGG (p.G319dup)
ISCN -
DB-ID ARID1B_000136 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARID1B NM_020732.3 -/. - c.942_944dup r.(?) p.(Gly319dup)


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