Variant #0000002809 (NC_000011.10:g.5226925C>G, NC_000011.10(NM_000518.4):c.92+5G>C (HBB))
Individual ID |
00000649 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.5226925C>G |
Published as |
- |
Reference |
Faidatul Syazlin Abdul Hamid et al.(2015): 10.4172/2155-9864.1000260 |
DB-ID |
HBB_000003 See all 32 reported entries |
dbSNP ID |
rs33915217 |
Frequency |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nur Aisyah Athirah |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nur Aisyah Athirah |
Date created |
2021-05-23 09:45:19 +08:00 (CST) |
Date last edited |
2021-08-18 14:38:08 +08:00 (CST) |

Variant on transcripts
Screenings
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