Variant #0000016295 (NC_000008.10:g.(100050795_100108539)_(100155394_100160068)dup, NC_000008.10(NM_017890.3):c.(291+1_292-1)_(1843+1_1844-1)dup (VPS13B))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(100050795_100108539)_(100155394_100160068)dup |
| DNA change (hg38) |
- |
| Published as |
dup ex4-13 |
| ISCN |
- |
| DB-ID |
VPS13B_000013 See all 2 reported entries |
| Variant remarks |
1 COH1 family (com-het) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-11-14 13:00:16 +01:00 (CET) |
| Date last edited |
2019-03-08 11:13:34 +01:00 (CET) |

Variant on transcripts
|