Variant #0000016291 (NC_000008.10:g.100026038_100026039delinsA, NM_017890.3:c.22_23delCCinsA (VPS13B))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.100026038_100026039delinsA |
| DNA change (hg38) |
g.99013810_99013811delinsA |
| Published as |
c.22_23delCCinsA: p.Pro8fsX3 |
| ISCN |
- |
| DB-ID |
VPS13B_000009 |
| Variant remarks |
1 Danish COH1 patient (com-het) |
| Reference |
PubMed: Kolehmainen et al. 2004 |
| 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 |
2017-05-05 18:33:04 +02:00 (CEST) |

Variant on transcripts
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