Variant #0000710807 (NC_000012.11:g.(90486683_90488249)_(90490259_90492571)del)
| Individual ID |
00324548 |
| Chromosome |
12 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(90486683_90488249)_(90490259_90492571)del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
chr12_007219 |
| Variant remarks |
<26kb deletion incl. rs12817868 and rs10858953 |
| Reference |
PubMed: Durlu 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2021-01-05 14:58:01 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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