Variant #0000547141 (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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
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