Variant #0000807829 (NC_000017.10:g.17697129_17697134dup, NM_030665.3:c.867_872dup (RAI1))
Chromosome |
17 |
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.17697129_17697134dup |
DNA change (hg38) |
- |
Published as |
RAI1(NM_030665.3):c.831_832insCAGCAG (p.(Asp277_Gln278insGlnGln)), RAI1(NM_030665.4):c.867_872dupGCAGCA (p.Q290_Q291dup) |
ISCN |
- |
DB-ID |
RAI1_000016 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 |
2021-09-17 14:40:49 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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