Variant #0000016296 (NC_000008.10:g.100108649_100108650insT, NM_017890.3:c.401_402insT (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.100108649_100108650insT |
| DNA change (hg38) |
g.99096421_99096422insT |
| Published as |
402insT |
| ISCN |
- |
| DB-ID |
VPS13B_000014 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 11:01:32 +01:00 (CET) |

Variant on transcripts
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