Variant #0000331297 (NC_000006.11:g.157100017_157100019del, NM_020732.3:c.954_956del (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.157100017_157100019del
DNA change (hg38) g.156778883_156778885del
Published as ARID1B(NM_001346813.1):c.954_956del (p.(Gly319del)), ARID1B(NM_001371656.1):c.1203_1205delAGG (p.G402del)
ISCN -
DB-ID ARID1B_000138 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 2023-04-16 21:50:28 +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.954_956del r.(?) p.(Gly319del)


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