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 |
No license selected |
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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|