Variant #0000016300 (NC_000008.10:g.100115235_100115238del, NM_017890.3:c.467_470delATAA (VPS13B))
Chromosome |
8 |
Allele |
Unknown |
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.100115235_100115238del |
DNA change (hg38) |
g.99103007_99103010del |
Published as |
c.463_466delATAA: p.Asn156fsX4 |
ISCN |
- |
DB-ID |
VPS13B_000018 |
Variant remarks |
1 British COH1 patient (hom) |
Reference |
PubMed: Kolehmainen et al. 2004 |
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 |
2020-06-24 14:14:26 +02:00 (CEST) |

Variant on transcripts
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