Variant #0000689664 (NC_000006.11:g.157099196_157099204del, NM_020732.3:c.133_141del (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.157099196_157099204del
DNA change (hg38) -
Published as ARID1B(NM_001346813.1):c.133_141delGCGGCGGCA (p.A45_A47del), ARID1B(NM_020732.3):c.133_141delGCGGCGGCA (p.A45_A47del)
ISCN -
DB-ID ARID1B_000328 See all 3 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-09-15 15:50:26 +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.382_390del r.(?) p.(Ala128_Ala130del)
ARID1B NM_020732.3 -/. - c.133_141del r.(?) p.(Ala45_Ala47del)


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