Variant #0000977058 (NC_000006.11:g.157100223_157100263del, NM_020732.3:c.1160_1200del (ARID1B))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.157100223_157100263del
DNA change (hg38) -
Published as ARID1B(NM_001371656.1):c.1409_1449del (p.A470Gfs*134)
ISCN -
DB-ID ARID1B_000458 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARID1B NM_001374828.1 +/. - c.1409_1449del r.(?) p.(Ala470Glyfs*134)
ARID1B NM_020732.3 +/. - c.1160_1200del r.(?) p.(Ala387Glyfs*134)


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