Variant #0000016305 (NC_000008.10:g.100146878G>T, NM_017890.3:c.1225G>T (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.100146878G>T |
| DNA change (hg38) |
g.99134650G>T |
| Published as |
c.1225g.t ( p.Glu409X ) |
| ISCN |
- |
| DB-ID |
VPS13B_000023 |
| Variant remarks |
1 Palestinian COH1 family (het) |
| Reference |
PubMed: Taban et al. 2007 |
| 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 19:04:32 +02:00 (CEST) |

Variant on transcripts
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