Variant #0000223342 (NC_000013.10:g.23756594G>A, NC_000013.10(NM_000231.2):c.-1+1380G>A (SGCG))
Chromosome |
13 |
Allele |
Parent #1 |
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.23756594G>A |
DNA change (hg38) |
g.23182455G>A |
Published as |
- |
ISCN |
- |
DB-ID |
SGCG_000015 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs3794371 |
Origin |
Germline |
Segregation |
- |
Frequency |
0.48 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2005-01-15 14:57:07 +01:00 (CET) |
Date last edited |
2012-11-02 20:43:04 +01:00 (CET) |

Variant on transcripts
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