Variant #0000658035 (NC_000017.10:g.11887531_11887534del, NC_000017.10(NM_144680.2):c.667-8_667-5del (ZNF18))
| 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.11887531_11887534del |
| DNA change (hg38) |
g.11984214_11984217del |
| Published as |
ZNF18(NM_144680.3):c.667-8_667-5delTTTT |
| ISCN |
- |
| DB-ID |
ZNF18_000004 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_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2020-07-13 08:51:53 +02:00 (CEST) |

Variant on transcripts
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