Variant #0000016289 (NC_000008.10:g.100001615_100141005del, NC_000008.10(NM_017890.3):c.-23990_1207-5855del (VPS13B))
Chromosome |
8 |
Allele |
Both (homozygous) |
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.100001615_100141005del |
DNA change (hg38) |
g.98989387_99128777del |
Published as |
Del promotor - 8: 100070791 - 100210181 bp (hg18) |
ISCN |
- |
DB-ID |
VPS13B_000007 |
Variant remarks |
2 Belgian COH1 families (hom); Deletion of exons 1-9a |
Reference |
PubMed: Balikova et al. 2009 |
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 |
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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