Variant #0000550167 (NC_000013.10:g.31789184_31789188del, NC_000013.10(NM_194318.3):c.71-4_71del (B3GLCT))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.31789184_31789188del |
DNA change (hg38) |
g.31215047_31215051del |
Published as |
B3GALTL(NM_194318.3):c.71-4_71del (p.?) |
ISCN |
- |
DB-ID |
B3GLCT_000054 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00012 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-07-03 14:38:47 +02:00 (CEST) |

Variant on transcripts
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