Variant #0000016290 (NC_000008.10:g.99945853_100278670del, NC_000008.10(NM_017890.3):c.-79752_2516-7756del (VPS13B))
Chromosome |
8 |
Allele |
Maternal (confirmed) |
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.99945853_100278670del |
DNA change (hg38) |
g.98933625_99266442del |
Published as |
315 kb del: exons 1-17: chr8(hg18):100015029...100347846; c.1-2515del |
ISCN |
- |
DB-ID |
VPS13B_000008 |
Variant remarks |
1 German/African COH1 family (com-het); Chr8(hg18):g.100015029_100347846del = Chr8(hg19):g.99945853_100278670del |
Reference |
Rivera-Brugués 2011 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
0/1612 CON |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Anne Polvi |
Database submission license |
No license selected |
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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