Variant #0000016296 (NC_000008.10:g.100108649_100108650insT, NM_017890.3:c.401_402insT (VPS13B))
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic (recessive) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.100108649_100108650insT |
DNA change (hg38) |
g.99096421_99096422insT |
Published as |
402insT |
ISCN |
- |
DB-ID |
VPS13B_000014 See all 2 reported entries |
Variant remarks |
1 COH1 family (com-het) |
Reference |
- |
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 |
2019-03-08 11:01:32 +01:00 (CET) |

Variant on transcripts
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