Variant #0000000933 (NC_000006.12:g.152219094G>T, NM_182961.3:c.21953C>A (SYNE1))
Individual ID |
00000188 |
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.152219094G>T |
Published as |
A7318E |
Reference |
Shafina-Nadiawati Abdul et al. (2017) |
DB-ID |
SYNE1_000006 |
dbSNP ID |
- |
Frequency |
1/9 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nuur Athirah Binti Mohd Daud |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nuur Athirah Binti Mohd Daud |
Date created |
2020-11-25 14:50:51 +08:00 (CST) |
Date last edited |
2020-12-14 17:01:20 +08:00 (CST) |

Variant on transcripts
Screenings
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