Variant #0000223276 (NC_000004.11:g.52904446del, NM_000232.4:c.-20del (SGCB))
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.52904446del |
DNA change (hg38) |
g.52038280del |
Published as |
-20delG |
ISCN |
- |
DB-ID |
SGCB_000085 |
Variant remarks |
- |
Reference |
from website {DBsub-Emory} |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Madhuri Hegde |
Database submission license |
No license selected |
Created by |
Madhuri Hegde |
Date created |
2012-10-26 15:19:20 +02:00 (CEST) |
Date last edited |
2020-06-16 13:00:06 +02:00 (CEST) |

Variant on transcripts
|