Variant #0000074055 (NC_000013.10:g.31843415G>A, NC_000013.10(NM_194318.3):c.660+1G>A (B3GLCT))
Chromosome |
13 |
Allele |
Paternal (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.31843415G>A |
DNA change (hg38) |
g.31269278G>A |
Published as |
1020+1G>A |
ISCN |
- |
DB-ID |
B3GLCT_000002 See all 32 reported entries |
Variant remarks |
- |
Reference |
PubMed: Lesnik Oberstein 2006, PubMed: Hess 2008 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00071 View details |
Owner |
Martine van Belzen |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |
Date created |
2006-08-10 16:30:11 +02:00 (CEST) |
Date last edited |
2020-07-03 14:39:05 +02:00 (CEST) |

Variant on transcripts
Screenings
|