Variant #0000000799 (NC_000011.10:g.5225905T>G, NC_000011.10(NM_000518.4):c.316-179A>C (HBB))
Individual ID |
00000162 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.5225905T>G |
Published as |
IVS II-672 (A>C) |
Reference |
dbSNP |
DB-ID |
HBB_000051 See all 2 reported entries |
dbSNP ID |
rs185607297 |
Frequency |
1 |
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 |
2020-11-19 14:56:13 +08:00 (CST) |
Date last edited |
2021-08-23 11:00:19 +08:00 (CST) |

Variant on transcripts
Screenings
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