Variant #0000548137 (NC_000012.11:g.46243903_46243906dup, NM_152641.2:c.1997_2000dup (ARID2))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46243903_46243906dup
DNA change (hg38) g.45850120_45850123dup
Published as ARID2(NM_152641.4):c.1997_2000dupAAAT (p.M667Ifs*41)
ISCN -
DB-ID ARID2_000021
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-02 14:56:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARID2 NM_152641.2 +?/. - c.1997_2000dup r.(?) p.(Met667IlefsTer41)


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