Variant #0013105168 (NC_000024.9:g.2655281C>T, NM_003140.2:c.364G>A (SRY))
Chromosome |
Y |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2655281C>T |
DB-ID |
- |
dbSNP ID |
rs771449441 |
gnomAD frequency |
1/62407 |
gnomAD homozygote count |
unknown |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Database submission license |
No license selected |
Created by |
LOVD |
Date created |
2017-02-27 00:00:00 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|
|