Variant #0000304228 (NC_000012.11:g.132633458_132633501del, NM_175066.3:c.-4638_-4595del (DDX51))
Chromosome |
12 |
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.132633458_132633501del |
DNA change (hg38) |
g.132148913_132148956del |
Published as |
NOC4L(NM_024078.1):c.901+18_901+61del (p.(=)), NOC4L(NM_024078.3):c.897_901+39del |
ISCN |
- |
DB-ID |
NOC4L_000003 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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
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