Variant #0000560496 (NC_000017.10:g.17697129_17697134del, NM_030665.3:c.867_872del (RAI1))
Chromosome |
17 |
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.17697129_17697134del |
DNA change (hg38) |
g.17793815_17793820del |
Published as |
RAI1(NM_030665.3):c.838_843del (p.(Gln282_Gln283del)), RAI1(NM_030665.3):c.867_872delGCAGCA (p.Q290_Q291del), RAI1(NM_030665.4):c.867_872delGCAGCA ... |
ISCN |
- |
DB-ID |
RAI1_000021 See all 4 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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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