Variant #0000029465 (NC_000008.10:g.100874030G>A, NM_017890.3:c.11146G>A (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.100874030G>A |
| DNA change (hg38) |
g.99861802G>A |
| Published as |
NM_152564:c.11071G>A |
| ISCN |
- |
| DB-ID |
VPS13B_000161 See all 6 reported entries |
| Variant remarks |
1 patient (com-het) with autism and COH1 like features |
| Reference |
PubMed: Yu al. 2013 |
| ClinVar ID |
- |
| dbSNP ID |
rs142476821 |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
1000g 0.230 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00241 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2014-02-04 13:50:04 +01:00 (CET) |
| Date last edited |
2017-05-05 18:33:04 +02:00 (CEST) |

Variant on transcripts
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