Variant #0000001113 (NC_000007.13:g.94257615G>A, SGCE(NM_001099401.1):c.289C>T)
Individual ID |
00001113 |
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94257615G>A |
Reference |
Zimprich A1, Grabowski M, Asmus F, Naumann M, Berg D, Bertram M, Scheidtmann K, Kern P, Winkelmann J, Müller-Myhsok B, Riedel L, Bauer M, Müller T, Castro M, Meitinger T, Strom TM, Gasser T.(2001) |
DB-ID |
SGCE_000001 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
Y Yang |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Y Yang |

Variant on transcripts
Screenings
|
|