Variant #0000655519 (NC_000006.11:g.157099420_157099425dup, NM_020732.3:c.357_362dup (ARID1B))
| Chromosome |
6 |
| 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.157099420_157099425dup |
| DNA change (hg38) |
g.156778286_156778291dup |
| Published as |
ARID1B(NM_001371656.1):c.606_611dupGCAGCA (p.Q213_Q214dup), ARID1B(NM_017519.2):c.357_362dupGCAGCA (p.(Gln120_Gln121dup)) |
| ISCN |
- |
| DB-ID |
ARID1B_000311 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 |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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