Variant #0000620597 (NC_000001.10:g.27023020_27023022dup, NM_006015.4:c.126_128dup (ARID1A))

Chromosome 1
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.27023020_27023022dup
DNA change (hg38) g.26696529_26696531dup
Published as ARID1A(NM_006015.4):c.126_128dup (p.(Ala45dup)), ARID1A(NM_006015.4):c.126_128dupGGC (p.A45dup), ARID1A(NM_006015.6):c.126_128dupGGC (p.A45dup)
ISCN -
DB-ID ARID1A_000103 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +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     
ARID1A NM_006015.4 -/. - c.126_128dup r.(?) p.(Ala45dup)


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