Variant #0000016390 (NC_000008.10:g.100832259A>G, NM_017890.3:c.8978A>G (VPS13B))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.100832259A>G |
| DNA change (hg38) |
g.99820031A>G |
| Published as |
c.8978A>G: p.Asn2993Ser |
| ISCN |
- |
| DB-ID |
VPS13B_000108 See all 9 reported entries |
| Variant remarks |
1 Belgian sib pair (hom) with COH1 |
| Reference |
PubMed: Kolehmainen et al. 2004 |
| ClinVar ID |
- |
| dbSNP ID |
rs28940272 |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00323 View details |
| 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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