Variant #0000860219 (NC_000006.11:g.157099349_157099375del, NM_020732.3:c.286_312del (ARID1B))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.157099349_157099375del
DNA change (hg38) -
Published as ARID1B(NM_001346813.1):c.286_312delCATGCCCACCACCTCCACCACCACCAC (p.H96_H104del), ARID1B(NM_001374828.1):c.535_561del (p.(His179_His187del))
ISCN -
DB-ID ARID1B_000385 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARID1B NM_001374828.1 ?/. - c.535_561del r.(?) p.(His179_His187del)
ARID1B NM_020732.3 ?/. - c.286_312del r.(?) p.(His96_His104del)


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