Variant #0000689667 (NC_000006.11:g.157099493_157099504del, NM_020732.3:c.430_441del (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.157099493_157099504del |
DNA change (hg38) |
- |
Published as |
ARID1B(NM_001346813.1):c.430_441delGGCGGCGGCGCG (p.G144_A147del), ARID1B(NM_001371656.1):c.679_690delGGCGGCGGCGCG (p.G227_A230del) |
ISCN |
- |
DB-ID |
ARID1B_000329 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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2020-09-15 15:50:26 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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