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 International |
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) |

Variant on transcripts
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